Rubber composition, and pneumatic tire

Abstract

Provided are a rubber composition achieving balanced improvement in processability, fuel economy, rubber strength, abrasion resistance, wet-grip performance, and handling stability, and a pneumatic tire including the composition. The rubber composition includes, per 100% by mass of a rubber component, at least 35% by mass of SR, the composition including a conjugated diene polymer and a silica having N₂SA of 40-400 m²/g, the polymer being obtained by polymerizing a monomer component including a conjugated diene compound and a silicon-containing vinyl compound using a polymerization initiator of formula (I):

##STR00001##
to produce a copolymer, and reacting a compound containing nitrogen and/or silicon atoms with an active terminal of the copolymer, wherein the amount of the diene polymer is 1-90% by mass and the amount of polyisoprene-based rubber is 0-40% by mass, each per 100% by mass of the rubber component, and the amount of the silica is 10-150 parts by mass per 100 parts by mass of the rubber component.

Description

TECHNICAL FIELD

The present invention relates to a rubber composition and a pneumatic tire formed from the rubber composition.

BACKGROUND ART

With the recent increase in concern about environmental issues, the demand on automobiles for better fuel economy is increasing. Better fuel economy is also being required of rubber compositions used for automotive tires. For example, rubber compositions containing a conjugated diene polymer (e.g., polybutadiene, butadiene-styrene copolymer) and a filler (e.g., carbon black, silica) are used for automotive tires.

Patent Literature 1 proposes an example of a method for improving the fuel economy; this method uses a diene rubber (modified rubber) that is modified by an organosilicon compound containing an amino group and an alkoxy group. Although the use of a modified rubber increases reaction efficiency between silica and rubber (polymer) to improve the fuel economy, it tends to increase the Mooney viscosity so that the processability tends to deteriorate. Thus, good fuel economy and good processability cannot be achieved simultaneously. Furthermore, the use of a modified rubber may lead to excessively tight bond between silica and rubber so that the rubber strength and the abrasion resistance may decrease.

Additionally, as rubber compositions for automobile tires need to be excellent in wet-grip performance and handling stability in view of safety, a technique is desired which achieves balanced improvements in these properties as well as fuel economy, processability, rubber strength and abrasion resistance at high levels.

CITATION LIST

Patent Literature

• Patent Literature 1: JP 2000-344955 A

SUMMARY OF INVENTION

Technical Problem

An object of the present invention is to solve the problems identified above by providing a rubber composition capable of achieves a balanced improvement in processability, fuel economy, rubber strength, abrasion resistance, wet-grip performance, and handling stability, and by providing a pneumatic tire formed from the rubber composition.

Solution to Problem

The present invention relates to a rubber composition, including, based on 100% by mass of a rubber component, not less than 35% by mass of styrene-butadiene rubber, the rubber composition comprising

a conjugated diene polymer, and

a silica having a nitrogen adsorption specific surface area of 40 to 400 m²/g,

the conjugated diene polymer being obtained by polymerizing a monomer component including a conjugated diene compound and a silicon-containing vinyl compound in the presence of a polymerization initiator represented by the following formula (I):

##STR00002##
wherein i represents 0 or 1; R¹¹ represents a C_1-100 hydrocarbylene group; R¹² and R¹³ each represent an optionally substituted hydrocarbyl group or a trihydrocarbylsilyl group, or R¹² and R¹³ are bonded to each other to form a hydrocarbylene group optionally containing at least one, as a hetero atom, selected from the group consisting of a silicon atom, a nitrogen atom, and an oxygen atom; and M represents an alkali metal atom, to produce a copolymer, and

then reacting a compound containing at least one of a nitrogen atom and a silicon atom with an active terminal of the copolymer,

wherein an amount of the conjugated diene polymer is 1 to 90% by mass and an amount of a polyisoprene-based rubber is 0 to 40% by mass, each based on 100% by mass of the rubber component, and

an amount of the silica is 10 to 150 parts by mass for each 100 parts by mass of the rubber component.

R¹¹ in the formula (I) is preferably a group represented by the following formula (Ia):

##STR00003##
wherein R¹⁴ represents a hydrocarbylene group including at least one of a structural unit derived from a conjugated diene compound and a structural unit derived from an aromatic vinyl compound; and n represents an integer of 1 to 10.

R¹⁴ in the formula (Ia) is preferably a hydrocarbylene group including from one to ten isoprene-derived structural unit(s).

The silicon-containing vinyl compound is preferably a compound represented by the following formula (II):

##STR00004##
wherein m represents 0 or 1; R²¹ represents a hydrocarbylene group; X¹, X², and X³ each represent a substituted amino group, a hydrocarbyloxy group, or an optionally substituted hydrocarbyl group.

The conjugated diene polymer preferably contains a structural unit derived from an aromatic vinyl compound.

The silica preferably includes silica (1) having a nitrogen adsorption specific surface area of at least 50 m²/g but less than 120 m²/g, and silica (2) having a nitrogen adsorption specific surface area of not less than 120 m²/g.

The rubber composition preferably includes a solid resin having a glass transition temperature of 60 to 120° C. in an amount of 1 to 30 parts by mass for each 100 parts by mass of the rubber component.

Preferably, the silica includes silica (1) having a nitrogen adsorption specific surface area of at least 50 m²/g but less than 120 m²/g, and silica (2) having a nitrogen adsorption specific surface area of not less than 120 m²/g, and the rubber composition includes a solid resin having a glass transition temperature of 60 to 120° C. in an amount of 1 to 30 parts by mass for each 100 parts by mass of the rubber component.

The rubber composition preferably includes a mercapto group-containing silane coupling agent in an amount of 0.5 to 20 parts by mass for each 100 parts by mass of the silica.

Preferably, the rubber composition includes a mercapto group-containing silane coupling agent in an amount of 0.5 to 20 parts by mass for each 100 parts by mass of the silica, and the silica includes silica (1) having a nitrogen adsorption specific surface area of at least 50 m²/g but less than 120 m²/g, and silica (2) having a nitrogen adsorption specific surface area of not less than 120 m²/g.

The rubber composition preferably includes a mercapto group-containing silane coupling agent in an amount of 0.5 to 20 parts by mass for each 100 parts by mass of the silica, and a solid resin having a glass transition temperature of 60 to 120° C. in an amount of 1 to 30 parts by mass for each 100 parts by mass of the rubber component.

Preferably, the rubber composition includes a mercapto group-containing silane coupling agent in an amount of 0.5 to 20 parts by mass for each 100 parts by mass of the silica, the silica includes silica (1) having a nitrogen adsorption specific surface area of at least 50 m²/g but less than 120 m²/g, and silica (2) having a nitrogen adsorption specific surface area of not less than 120 m²/g, and the rubber composition includes a solid resin having a glass transition temperature of 60 to 120° C. in an amount of 1 to 30 parts by mass for each 100 parts by mass of the rubber component.

Preferably, the rubber composition includes a mercapto group-containing silane coupling agent in an amount of 0.5 to 20 parts by mass for each 100 parts by mass of the silica, and

the silane coupling agent is at least one of a compound represented by the formula (1) below, and a compound containing a linking unit A represented by the formula (2) below and a linking unit B represented by the formula (3) below,

##STR00005##
wherein R¹⁰¹ to R¹⁰³ each represent a branched or unbranched C_1-12 alkyl group, a branched or unbranched C_1-12 alkoxy group, or a group represented by —O—(R¹¹¹—O)_z—R¹¹² where z R¹¹¹s each represent a branched or unbranched C_1-30 divalent hydrocarbon group, and z R¹¹¹s may be the same as or different from one another; R¹¹² represents a branched or unbranched C_1-30 alkyl group, a branched or unbranched C_2-30 alkenyl group, a C_6-30 aryl group, or a C_7-30 aralkyl group; and z represents an integer of 1 to 30, and R¹⁰¹ to R¹⁰³ may be the same as or different from one another; and R¹⁰⁴ represents a branched or unbranched C_1-6 alkylene group;

##STR00006##
wherein R²⁰¹ represents a hydrogen atom, a halogen atom, a branched or unbranched C_1-30 alkyl group, a branched or unbranched C_2-30 alkenyl group, a branched or unbranched C_2-30 alkynyl group, or the alkyl group in which a terminal hydrogen atom is replaced with a hydroxyl group or a carboxyl group; R²⁰² represents a branched or unbranched C_1-30 alkylene group, a branched or unbranched C_2-30 alkenylene group, or a branched or unbranched C_2-30 alkynylene group; and R²⁰¹ and R²⁰² may be joined together to form a cyclic structure.

Preferably, the silica includes silica (1) having a nitrogen adsorption specific surface area of at least 50 m²/g but less than 120 m²/g, and silica (2) having a nitrogen adsorption specific surface area of not less than 120 m²/g, and

the nitrogen adsorption specific surface areas and amounts of the silica (1) and the silica (2) satisfy the following inequalities:
(Nitrogen adsorption specific surface area of silica (2))/(Nitrogen adsorption specific surface area of silica (1))≧1.4, and
(Amount of silica (1))×0.06≦(Amount of silica (2))≦(Amount of silica (1))×15.

Preferably, the rubber composition includes at least one of

at least one liquid resin having a glass transition temperature of −40 to 20° C. selected from the group consisting of aromatic petroleum resins, terpene resins, and rosin resins, and

a plasticizer having a glass transition temperature of −40 to 20° C., and

a combined amount of the liquid resin and the plasticizer is 1 to 30 parts by mass for each 100 parts by mass of the rubber component.

The rubber composition preferably has a tan δ peak temperature of not lower than −16° C.

The rubber composition is preferably for use in a tread.

The present invention also relates to a pneumatic tire, formed from the rubber composition.

Advantageous Effects of Invention

The rubber composition of the present invention is a rubber composition including a specific amount of styrene-butadiene rubber together with a specific amount of a specific conjugated diene polymer and a specific amount of a specific silica. Thus, the rubber composition enables to provide a pneumatic tire that achieves a balanced improvement in processability, fuel economy, rubber strength, abrasion resistance, wet-grip performance, and handling stability (particularly, handling stability on dry road surface).

DESCRIPTION OF EMBODIMENTS

As used herein, the hydrocarbyl group denotes a monovalent group provided by removing one hydrogen atom from a hydrocarbon; the hydrocarbylene group denotes a divalent group provided by removing two hydrogen atoms from a hydrocarbon; the hydrocarbyloxy group denotes a monovalent group provided by replacing the hydrogen atom of a hydroxyl group with a hydrocarbyl group; the substituted amino group denotes a group provided by replacing at least one hydrogen atom of an amino group with a monovalent atom other than a hydrogen atom or with a monovalent group, or denotes a group provided by replacing two hydrogen atoms of an amino group with a divalent group; the hydrocarbyl group having a substituent (hereinafter, also referred to as substituted hydrocarbyl group) denotes a monovalent group provided by replacing at least one hydrogen atom of a hydrocarbyl group with a substituent; and the hydrocarbylene group containing a hetero atom (hereinafter, also referred to as hetero atom-containing hydrocarbylene group) denotes a divalent group provided by replacing a hydrogen atom and/or a carbon atom other than the carbon atoms from which a hydrogen atom has been removed in a hydrocarbylene group with a group containing a hetero atom (an atom other than carbon and hydrogen atoms).

The conjugated diene polymer according to the present invention is obtained by

polymerizing a monomer component including a conjugated diene compound and a silicon-containing vinyl compound in the presence of a polymerization initiator represented by the following formula (I):

##STR00007##
wherein i represents 0 or 1; R¹¹ represents a C_1-100 hydrocarbylene group; R¹² and R¹³ each represent an optionally substituted hydrocarbyl group or a trihydrocarbylsilyl group, or R¹² and R¹³ are bonded to each other to form a hydrocarbylene group optionally containing at least one, as a hetero atom, selected from the group consisting of a silicon atom, a nitrogen atom, and an oxygen atom; and M represents an alkali metal atom, to produce a copolymer, and

then reacting a compound containing a nitrogen atom and/or a silicon atom with an active terminal of the copolymer.

As used herein, the term “modifying” means bonding a copolymer containing a diene compound, or a copolymer containing a diene compound and an aromatic vinyl compound, to a compound other than the compound(s). The above conjugated diene polymer has a structure in which a polymerization initiation terminal is modified by the polymerization initiator represented by the formula (I); a main chain is modified by copolymerization with a silicon-containing vinyl compound; and a termination terminal is modified by a compound containing a nitrogen atom and/or a silicon atom, a silicon-containing vinyl compound. Use of the conjugated diene polymer in combination with other rubbers (e.g. polyisoprene-based rubbers) enables to disperse silica well and achieve a balanced improvement in fuel economy, rubber strength, abrasion resistance, wet-grip performance, and handling stability. In general, the use of a modified rubber in which all of an initiation terminal, a main chain and a termination terminal are modified tends to greatly deteriorate the processability. In contrast, the use of the conjugated diene polymer in which each of an initiation terminal, a main chain and a termination terminal is modified by a specific compound enables to ensure good processability, and furthermore, enables to synergistically enhance the effects of improving the fuel economy, rubber strength, abrasion resistance, wet-grip performance, and handling stability. Thus, balanced improvements in processability, fuel economy, rubber strength, abrasion resistance, wet-grip performance, and handling stability can be achieved at high levels.

In the formula (I), i is 0 or 1, and preferably 1.

R¹¹ in the formula (I) is a C_1-100 hydrocarbylene group, preferably a C_6-100 hydrocarbylene group, and more preferably a C_7-80 hydrocarbylene group. If the R¹¹ has more than 100 carbon atoms, the polymerization initiator has an increased molecular weight, which may reduce the cost efficiency and the handleability during the polymerization.

Plural kinds of compounds different in the carbon number of R¹¹ may be used in combination as the polymerization initiator represented by the formula (I).

R¹¹ in the formula (I) is preferably a group represented by the following formula (Ia):

##STR00008##
wherein R¹⁴ represents a hydrocarbylene group including at least one of a structural unit derived from a conjugated diene compound and a structural unit derived from an aromatic vinyl compound; and n represents an integer of 1 to 10.

R¹⁴ in the formula (Ia) represents a hydrocarbylene group including at least one of a structural unit derived from a conjugated diene compound and a structural unit derived from an aromatic vinyl compound, preferably a hydrocarbylene group including an isoprene-derived structural unit, and more preferably a hydrocarbylene group including from one to ten isoprene-derived structural unit(s).

The number of at least one of the structural unit derived from a conjugated diene compound and the structural unit derived from an aromatic vinyl compound in R¹⁴ is preferably from one to ten, and more preferably from one to five.

In the formula (Ia), n represents an integer of 1 to 10, and preferably an integer of 2 to 4.

Examples of R¹¹ include a group obtained by bonding from one to ten isoprene-derived structural unit(s) and a methylene group, a group obtained by bonding from one to ten isoprene-derived structural unit(s) and an ethylene group, and a group obtained by bonding from one to ten isoprene-derived structural unit(s) and a trimethylene group; and preferably a group obtained by bonding from one to ten isoprene-derived structural unit(s) and a trimethylene group.

In the formula (I), R¹² and R¹³ each are an optionally substituted hydrocarbyl group or a trihydrocarbylsilyl group, or R¹² and R¹³ are bonded to each other to form a hydrocarbylene group optionally containing at least one, as a hetero atom, selected from the group consisting of a silicon atom, a nitrogen atom, and an oxygen atom.

The optionally substituted hydrocarbyl group is a hydrocarbyl group or substituted hydrocarbyl group. Examples of the substituent in the substituted hydrocarbyl group include a substituted amino group and a hydrocarbyloxy group. Examples of the hydrocarbyl group include acyclic alkyl groups such as a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, an isobutyl group, a sec-butyl group, a tert-butyl group, an n-pentyl group, an n-hexyl group, an n-octyl group, and an n-dodecyl group; cyclic alkyl groups such as a cyclopentyl group and a cyclohexyl group; and aryl groups such as a phenyl group and a benzyl group, and preferably acyclic alkyl groups, and more preferably C_1-4 acyclic alkyl groups. Examples of the substituted hydrocarbyl group in which the substituent is a substituted amino group include an N,N-dimethylaminomethyl group, a 2-N,N-dimethylaminoethyl group, and a 3-N,N-dimethylaminopropyl group. Examples of the substituted hydrocarbyl group in which the substituent is a hydrocarbyloxy group include a methoxymethyl group, a methoxyethyl group, and an ethoxymethyl group. Among the above examples, a hydrocarbyl group is preferable; a C_1-4 acyclic alkyl group is more preferable; and a methyl group or an ethyl group is still more preferable.

Examples of the trihydrocarbylsilyl group include a trimethylsilyl group, and a tert-butyl-dimethylsilyl group. A trimethylsilyl group is preferable.

The hydrocarbylene group optionally containing at least one, as a hetero atom, selected from the group consisting of a silicon atom, a nitrogen atom, and an oxygen atom is a hydrocarbylene group, or a hetero atom-containing hydrocarbylene group in which the hetero atom is at least one selected from the group consisting of a silicon atom, a nitrogen atom and an oxygen atom. Examples of the hetero atom-containing hydrocarbylene group in which the hetero atom is at least one selected from the group consisting of a silicon atom, a nitrogen atom and an oxygen atom include a hetero atom-containing hydrocarbylene group in which the hetero atom is a silicon atom, a hetero atom-containing hydrocarbylene group in which the hetero atom is a nitrogen atom, and a hetero atom-containing hydrocarbylene group in which the hetero atom is an oxygen atom. Examples of the hydrocarbylene group include alkylene groups such as a tetramethylene group, a pentamethylene group, a hexamethylene group, a pent-2-ene-1,5-diyl group, and a 2,2,4-trimethylhexane-1,6-diyl group; and alkenediyl groups such as a pent-2-ene-1,5-diyl group, and preferably alkylene groups, and more preferably C_4-7 alkylene groups. Examples of the hetero atom-containing hydrocarbylene group in which the hetero atom is a silicon atom include a group represented by —Si(CH₃)₂—CH₂—CH₂—Si(CH₃)₂—. Examples of the hetero atom-containing hydrocarbylene group in which the hetero atom is a nitrogen atom include a group represented by —CH═N—CH═CH— and a group represented by —CH═N—CH₂—CH₂—. Examples of the hetero atom-containing hydrocarbylene group in which the hetero atom is an oxygen atom include a group represented by —CH₂—CH₂—O—CH₂—CH₂—. Among the above examples, a hydrocarbylene group is preferable; a C_4-7 alkylene group is more preferable; and a tetramethylene group, a pentamethylene group, and a hexamethylene group are still more preferable.

Preferably, R¹² and R¹³ each are a hydrocarbyl group, or R¹² and R¹³ are bonded to each other to form a hydrocarbylene group. More preferably, R¹² and R¹³ each are a acyclic alkyl group, or R¹² and R¹³ are bonded to each other to form a C_4-7 alkylene group. Still more preferably, R¹² and R¹³ each are a methyl group or an ethyl group.

M in the formula (I) represents an alkali metal atom. Examples of the alkali metal atom include Li, Na, K, and Cs; and a preferable example thereof is Li.

The polymerization initiator represented by the formula (I) in which i is 1 may be a compound formed from one to five isoprene-derived structural unit(s) polymerized with an aminoalkyllithium compound. Examples of the aminoalkyllithium compound include N,N-dialkylaminoalkyllithiums such as 3-(N,N-dimethylamino)-1-propyllithium, 3-(N,N-diethylamino)-1-propyllithium, 3-(N,N-di-n-butylamino)-1-propyllithium, 4-(N,N-dimethylamino)-1-butyllithium, 4-(N,N-diethylamino)-1-butyllithium, 4-(N,N-di-n-propylamino)-1-butyllithium, and 3-(N,N-di-n-butylamino)-1-butyllithium; hetero atom-free cyclic aminoalkyllithium compounds such as 3-(1-pyrrolidino)-1-propyllithium, 3-(1-piperidino)-1-propyllithium, 3-(1-hexamethyleneimino)-1-propyllithium, and 3-[1-(1,2,3,6-tetrahydropyridino)]-1-propyllithium; and hetero atom-containing cyclic aminoalkyllithium compounds such as 3-(1-morpholino)-1-propyllithium, 3-(1-imidazolyl)-1-propyllithium, 3-(4,5-dihydro-1-imidazolyl)-1-propyllithium, and 3-(2,2,5,5-tetramethyl-1-aza-2,5-disila-1-cyclopentyl)-1-propyllithium, and preferably N,N-dialkylaminoalkyllithium, and more preferably 3-(N,N-dimethylamino)-1-propyllithium or 3-(N,N-diethylamino)-1-propyllithium.

Examples of the polymerization initiator represented by the formula (I) in which i is 0 include lithium hexamethyleneimide, lithium pyrrolidide, lithium piperidide, lithium heptamethyleneimide, lithium dodecamethyleneimide, lithium dimethylamide, lithium diethylamide, lithium dipropylamide, lithium dibutylamide, lithium dihexylamide, lithium diheptylamide, lithium dioctylamide, lithium di-2-ethylhexylamide, lithium didecylamide, lithium-N-methylpiperadide, lithium ethylpropylamide, lithium ethylbutylamide, lithium methylbutylamide, lithium ethylbenzylamide, and lithium methylphenethylamide.

The polymerization initiator represented by the formula (I) in which i is 0 may be prepared in advance from a secondary amine and a hydrocarbyllithium compound before it is used for the polymerization reaction, or may be prepared in the polymerization system. Examples of the secondary amine include dimethylamine, diethylamine, dibutylamine, dioctylamine, dicyclohexylamine, and diisobutylamine. Other examples thereof include cyclic amines, such as azacycloheptane (i.e. hexamethyleneimine), 2-(2-ethylhexyl)pyrrolidine, 3-(2-propyl)pyrrolidine, 3,5-bis(2-ethylhexyl)piperidine, 4-phenylpiperidine, 7-decyl-1-azacyclotridecane, 3,3-dimethyl-1-azacyclotetradecane, 4-dodecyl-1-azacyclooctane, 4-(2-phenylbutyl)-1-azacyclooctane, 3-ethyl-5-cyclohexyl-1-azacycloheptane, 4-hexyl-1-azacycloheptane, 9-isoamyl-1-azacycloheptadecane, 2-methyl-1-azacycloheptadec-9-ene, 3-isobutyl-1-azacyclododecane, 2-methyl-7-t-butyl-1-azacyclododecane, 5-nonyl-1-azacyclododecane, 8-(4-methylphenyl)-5-pentyl-3-azabicyclo[5.4.0]undecane, 1-butyl-6-azabicyclo[3.2.1]octane, 8-ethyl-3-azabicyclo[3.2.1]octane, 1-propyl-3-azabicyclo[3.2.2]nonane, 3-(t-butyl)-7-azabicyclo[4.3.0]nonane, and 1,5,5-trimethyl-3-azabicyclo[4.4.0]decane.

The polymerization initiator represented by the formula (I) is preferably a compound in which i is 1, more preferably a compound formed from one to five isoprene-derived structural unit(s) polymerized with N,N-aminoalkyllithium, and still more preferably a compound formed from one to five isoprene-derived structural unit(s) polymerized with 3-(N,N-dimethylamino)-1-propyllithium or 3-(N,N-diethylamino)-1-propyllithium.

The amount of the polymerization initiator represented by the formula (1) to be used is preferably 0.01 to 15 mmol, and more preferably 0.1 to 10 mmol, for each 100 g of the monomer component used in the polymerization.

In the present invention, other polymerization initiators, such as n-butyllithium, may be used in combination, if necessary.

Examples of the conjugated diene compound include 1,3-butadiene, isoprene, 1,3-pentadiene, 2,3-dimethyl-1,3-butadiene, 1,3-hexadiene, and myrcene. Any of these may be used alone or two or more of these may be used in combination. In view of easy availability, the conjugated diene compound is preferably 1,3-butadiene or isoprene.

The silicon-containing vinyl compound is preferably a compound represented by the following formula (II):

##STR00009##
wherein m represents 0 or 1; R²¹ represents a hydrocarbylene group; X¹, X², and X³ each represent a substituted amino group, a hydrocarbyloxy group, or an optionally substituted hydrocarbyl group.

Here, m in the formula (II) is 0 or 1, and preferably 0.

Examples of the hydrocarbylene group in the formula (II) include an alkylene group, an alkenediyl group, an arylene group, and a group in which an arylene group and an alkylene group are bonded. Examples of the alkylene group include a methylene group, an ethylene group, and a trimethylene group. Examples of the alkenediyl group include a vinylene group and an ethylene-1,1-diyl group. Examples of the arylene group include a phenylene group, a naphthylene group, and a biphenylene group. Examples of the group in which an arylene group and an alkylene group are bonded include a group in which a phenylene group and a methylene group are bonded, and a group in which a phenylene group and an ethylene group are bonded.

R²¹ is preferably an arylene group, and more preferably a phenylene group.

In the formula (II), X¹, X² and X³ each are a substituted amino group, a hydrocarbyloxy group, or an optionally substituted hydrocarbyl group. Preferably, at least one of X¹, X² and X³ is a substituted amino group. More preferably, two of X¹, X² and X³ are substituted amino groups.

In the formula (II), the substituted amino group is preferably a group represented by the following formula (IIa):

##STR00010##
wherein R²² and R²³ each represent an optionally substituted hydrocarbyl group or a trihydrocarbylsilyl group, or R²² and R²³ are bonded to each other to form a hydrocarbylene group optionally containing, as a hetero atom, a nitrogen atom and/or an oxygen atom.

The optionally substituted hydrocarbyl group in the formula (IIa) is a hydrocarbyl group or a substituted hydrocarbyl group. Examples of the substituted hydrocarbyl group include a substituted hydrocarbyl group in which the substituent is a hydrocarbyloxy group. Examples of the hydrocarbyl group include acyclic alkyl groups such as a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, an isobutyl group, a sec-butyl group, a tert-butyl group, an n-pentyl group, an n-hexyl group, and an n-octyl group; cyclic alkyl groups such as a cyclopentyl group and a cyclohexyl group; and aryl groups such as a phenyl group, a benzyl group, and a naphthyl group. The hydrocarbyl group is preferably a acyclic alkyl group, and more preferably a methyl group or an ethyl group. Examples of the substituted hydrocarbyl group in which the substituent is a hydrocarbyloxy group include alkoxyalkyl groups such as a methoxymethyl group, an ethoxymethyl group, and a methoxyethyl group; and aryloxyalkyl groups such as a phenoxymethyl group.

Examples of the trihydrocarbylsilyl group in the formula (IIa) include trialkylsilyl groups such as a trimethylsilyl group, a triethylsilyl group, and a tert-butyldimethylsilyl group.

The hydrocarbylene group optionally containing, as a hetero atom, a nitrogen atom and/or an oxygen atom in the formula (IIa) is a hydrocarbylene group, or a hetero atom-containing hydrocarbylene group in which the hetero atom is a nitrogen atom and/or an oxygen atom. Examples of the hetero atom-containing hydrocarbylene group in which the hetero atom is a nitrogen atom and/or an oxygen atom include a hydrocarbylene group containing a nitrogen atom as a hetero atom, and a hydrocarbylene group containing an oxygen atom as a hetero atom. Examples of the hydrocarbylene group include alkylene groups such as a trimethylene group, a tetramethylene group, a pentamethylene group, a hexamethylene group, a heptamethylene group, an octamethylene group, a decamethylene group, a dodecamethylene group, and a 2,2,4-trimethylhexane-1,6-diyl group; and alkenediyl groups such as a pent-2-ene-1,5-diyl group. Examples of the hetero atom-containing hydrocarbylene group in which the hetero atom is a nitrogen atom include a group represented by —CH═N—CH═CH— and a group represented by —CH═N—CH₂—CH₂—. Examples of the hetero atom-containing hydrocarbylene group in which the hetero atom is an oxygen atom include a group represented by —CH₂—CH₂—O—CH₂—CH₂—.

Preferably, R²² and R²³ each are an alkyl group, or R²² and R²³ are bonded to each other to form an alkylene group. R²² and R²³ each are more preferably an alkyl group, and still more preferably a methyl group or an ethyl group.

Examples of the substituted amino group represented by the formula (IIa) in which R²² and R²³ each are a hydrocarbyl group include dialkylamino groups such as a dimethylamino group, a diethylamino group, an ethylmethylamino group, a di-n-propylamino group, a diisopropylamino group, a di-n-butylamino group, a diisobutylamino group, a di-sec-butylamino group, and a di-tert-butylamino group; and diarylamino groups such as a diphenylamino group. Preferable examples thereof include dialkylamino groups, and more preferable examples thereof include dimethylamino groups, diethylamino groups, and di-n-butylamino groups. Examples of the substituted amino group in which R²² and R²³ each are a substituted hydrocarbyl group in which the substituent is a hydrocarbyloxy group include di(alkoxyalkyl)amino groups such as a di(methoxymethyl)amino group and a di(ethoxymethyl)amino group. Examples of the substituted amino group in which R²² and R²³ each are a trihydrocarbylsilyl group include trialkylsilyl group-containing amino groups such as a bis(trimethylsilyl)amino group, a bis(tert-butyldimethylsilyl)amino group, and an N-trimethylsilyl-N-methylamino group.

Examples of the substituted amino group represented by the formula (IIa) in which R²² and R²³ are bonded to each other to form a hydrocarbylene group include 1-alkyleneimino groups such as a 1-trimethyleneimino group, a 1-pyrrolidino group, a 1-piperidino group, a 1-hexamethyleneimino group, a 1-heptamethyleneimino group, a 1-octamethyleneimino group, a 1-decamethyleneimino group, and a 1-dodecamethyleneimino group. Examples of the substituted amino group in which R²² and R²³ are bonded to each other to form a hydrocarbylene group containing a nitrogen atom as a hetero atom include a 1-imidazolyl group and a 4,5-dihydro-1-imidazolyl group. Examples of the substituted amino group in which R²² and R²³ are bonded to each other to form a hydrocarbylene group containing an oxygen atom as a hetero atom include a morpholino group.

The substituted amino group represented by the formula (IIa) is preferably a dialkylamino group or a 1-alkyleneimino group; more preferably a dialkylamino group; and still more preferably a dimethylamino group, a diethylamino group, or a di-n-butylamino group.

Examples of the hydrocarbyloxy group in the formula (II) include alkoxy groups such as a methoxy group, an ethoxy group, an n-propoxy group, an isopropoxy group, an n-butoxy group, a sec-butoxy group, and a tert-butoxy group; and aryloxy groups such as a phenoxy group and a benzyloxy group.

The optionally substituted hydrocarbyl group in the formula (II) is a hydrocarbyl group or a substituted hydrocarbyl group. Examples of the substituted hydrocarbyl group include a substituted hydrocarbyl group in which the substituent is a hydrocarbyloxy group. Examples of the hydrocarbyl group include alkyl groups such as a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, a sec-butyl group, and a tert-butyl group; and aryl groups such as a phenyl group, a 4-methyl-1-phenyl group, and a benzyl group. Examples of the substituted hydrocarbyl group in which the substituent is a hydrocarbyloxy group include alkoxyalkyl groups such as a methoxymethyl group, an ethoxymethyl group, and an ethoxyethyl group.

Examples of the silicon-containing vinyl compound represented by the formula (II) in which one of X¹, X², and X³ is a substituted amino group, and m is 0 include (dialkylamino)dialkylvinylsilanes such as (dimethylamino)dimethylvinylsilane, (ethylmethylamino)dimethylvinylsilane, (di-n-propylamino)dimethylvinylsilane, (diisopropylamino)dimethylvinylsilane, (dimethylamino)diethylvinylsilane, (ethylmethylamino)diethylvinylsilane, (di-n-propylamino) diethylvinylsilane, and (diisopropylamino)diethylvinylsilane; [bis(trialkylsilyl)amino]dialkylvinylsilanes such as [bis(trimethylsilyl)amino]dimethylvinylsilane, [bis(t-butyldimethylsilyl)amino]dimethylvinylsilane, [bis(trimethylsilyl)amino]diethylvinylsilane, and [bis(t-butyldimethylsilyl)amino]diethylvinylsilane; (dialkylamino)di(alkoxyalkyl)vinylsilanes such as (dimethylamino)di(methoxymethyl)vinylsilane, (dimethylamino)di(methoxyethyl)vinylsilane, (dimethylamino)di(ethoxymethyl)vinylsilane, (dimethylamino)di(ethoxyethyl)vinylsilane, (diethylamino)di(methoxymethyl)vinylsilane, (diethylamino)di(methoxyethyl)vinylsilane, (diethylamino)di(ethoxymethyl)vinylsilane, and (diethylamino)di(ethoxyethyl)vinylsilane; and cyclic aminodialkylvinylsilane compounds such as pyrrolidinodimethylvinylsilane, piperidinodimethylvinylsilane, hexamethyleneiminodimethylvinylsilane, 4,5-dihydro-imidazolyldimethylvinylsilane, and morpholinodimethylvinylsilane.

Examples of the silicon-containing vinyl compound represented by the formula (II) in which one of X¹, X², and X³ is a substituted amino group, and m is 1 include (dialkylamino)dialkylvinylphenylsilanes such as (dimethylamino)dimethyl-4-vinylphenylsilane, (dimethylamino)dimethyl-3-vinylphenylsilane, (diethylamino)dimethyl-4-vinylphenylsilane, (diethylamino)dimethyl-3-vinylphenylsilane, (di-n-propylamino)dimethyl-4-vinylphenylsilane, (di-n-propylamino)dimethyl-3-vinylphenylsilane, (di-n-butylamino)dimethyl-4-vinylphenylsilane, (di-n-butylamino)dimethyl-3-vinylphenylsilane, (dimethylamino)diethyl-4-vinylphenylsilane, (dimethylamino)diethyl-3-vinylphenylsilane, (diethylamino)diethyl-4-vinylphenylsilane, (diethylamino)diethyl-3-vinylphenylsilane, (di-n-propylamino)diethyl-4-vinylphenylsilane, (di-n-propylamino)diethyl-3-vinylphenylsilane, (di-n-butylamino)diethyl-4-vinylphenylsilane, and (di-n-butylamino)diethyl-3-vinylphenylsilane.

Examples of the silicon-containing vinyl compound represented by the formula (II) in which two of X¹, X², and X³ each are a substituted amino group, and m is 0 include bis(dialkylamino)alkylvinylsilanes such as bis(dimethylamino)methylvinylsilane, bis(diethylamino)methylvinylsilane, bis(di-n-propylamino)methylvinylsilane, bis(di-n-butylamino)methylvinylsilane, bis(dimethylamino)ethylvinylsilane, bis(diethylamino)ethylvinylsilane, bis(di-n-propylamino)ethylvinylsilane, and bis(di-n-butylamino)ethylvinylsilane; bis[bis(trialkylsilyl)amino]alkylvinylsilanes such as bis[bis(trimethylsilyl)amino]methylvinylsilane, bis[bis(tert-butyldimethylsilyl)amino]methylvinylsilane, bis[bis(trimethylsilyl)amino]ethylvinylsilane, and bis[bis(tert-butyldimethylsilyl)amino]ethylvinylsilane; bis(dialkylamino)alkoxyalkylsilanes such as bis(dimethylamino)methoxymethylvinylsilane, bis(dimethylamino)methoxyethylvinylsilane, bis(dimethylamino)ethoxymethylvinylsilane, bis(dimethylamino)ethoxyethylvinylsilane, bis(diethylamino)methoxymethylvinylsilane, bis(diethylamino)methoxyethylvinylsilane, bis(diethylamino)ethoxymethylvinylsilane, and bis(dimethylamino)ethoxyethylvinylsilane; and bis(cyclic amino)alkylvinylsilane compounds such as bis(pyrrolidino)methylvinylsilane, bis(piperidino)methylvinylsilane, bis(hexamethyleneimino)methylvinylsilane, bis(4,5-dihydroimidazolyl)methylvinylsilane, and bis(morpholino)methylvinylsilane.

Examples of the silicon-containing vinyl compound represented by the formula (II) in which two of X¹, X², and X³ each are a substituted amino group, and m is 1 include bis(dialkylamino)alkylvinylphenylsilanes such as bis(dimethylamino)methyl-4-vinylphenylsilane, bis(dimethylamino)methyl-3-vinylphenylsilane, bis(diethylamino)methyl-4-vinylphenylsilane, bis(diethylamino)methyl-3-vinylphenylsilane, bis(di-n-propylamino)methyl-4-vinylphenylsilane, bis(di-n-propylamino)methyl-3-vinylphenylsilane, bis(di-n-butylamino)methyl-4-vinylphenylsilane, bis(di-n-butylamino)methyl-3-vinylphenylsilane, bis(dimethylamino)ethyl-4-vinylphenylsilane, bis(dimethylamino)ethyl-3-vinylphenylsilane, bis(diethylamino)ethyl-4-vinylphenylsilane, bis(diethylamino)ethyl-3-vinylphenylsilane, bis(di-n-propylamino)ethyl-4-vinylphenylsilane, bis(di-n-propylamino)ethyl-3-vinylphenylsilane, bis(di-n-butylamino)ethyl-4-vinylphenylsilane, and bis(di-n-butylamino)ethyl-3-vinylphenylsilane.

Examples of the silicon-containing vinyl compound represented by the formula (II) in which three of X¹, X², and X³ each are a substituted amino group, and m is 0 include tris(dialkylamino)vinylsilanes such as tris(dimethylamino)vinylsilane, tris(diethylamino)vinylsilane, tris(di-n-propylamino)vinylsilane, and tris(di-n-butylamino)vinylsilane.

Examples of the silicon-containing vinyl compound represented by the formula (II) in which three of X¹, X², and X³ each are a substituted amino group, and m is 1 include tris(dialkylamino)vinylphenylsilanes such as tris(dimethylamino)-4-vinylphenylsilane, tris(dimethylamino)-3-vinylphenylsilane, tris(diethylamino)-4-vinylphenylsilane, tris(diethylamino)-3-vinylphenylsilane, tris(di-n-propylamino)-4-vinylphenylsilane, tris(di-n-propylamino)-3-vinylphenylsilane, tris(di-n-butylamino)-4-vinylphenylsilane, and tris(di-n-butylamino)-3-vinylphenylsilane.

Examples of the silicon-containing vinyl compound represented by the formula (II) in which X¹, X², and X³ are not a substituted amino group, and m is 0 include trialkoxyvinylsilanes such as trimethoxyvinylsilane, triethoxyvinylsilane, and tripropoxyvinylsilane; dialkoxyalkylvinylsilanes such as methyldimethoxyvinylsilane and methyldiethoxyvinylsilane; dialkoxyarylvinylsilanes such as di(tert-pentoxy)phenylvinylsilane and di(tert-butoxy)phenylvinylsilane; monoalkoxydialkylvinylsilanes such as dimethylmethoxyvinylsilane; monoalkoxydiarylvinylsilanes such as tert-butoxydiphenylvinylsilane and tert-pentoxydiphenylvinylsilane; monoalkoxyalkylarylvinylsilanes such as tert-butoxymethylphenylvinylsilane and tert-butoxyethylphenylvinylsilane; and substituted alkoxyvinylsilane compounds such as tris(β-methoxyethoxy)vinylsilane.

Moreover, examples of the silicon-containing vinyl compound include bis(trialkylsilyl)-aminostyrenes such as 4-N,N-bis(trimethylsilyl)aminostyrene and 3-N,N-bis(trimethylsilyl)aminostyrene; and bis(trialkylsilyl)aminoalkylstyrenes such as 4-bis(trimethylsilyl)aminomethylstyrene, 3-bis(trimethylsilyl)aminomethylstyrene, 4-bis(trimethylsilyl)aminoethylstyrene, and 3-bis(trimethylsilyl)aminoethylstyrene.

The silicon-containing vinyl compound is preferably a compound represented by the formula (II), more preferably a compound represented by the formula (II) in which m is 0, and still more preferably a compound represented by the formula (II) in which two of X¹, X² and X³ are dialkyl amino groups.

The silicon-containing vinyl compound is particularly preferably bis(dimethylamino)methylvinylsilane, bis(diethylamino)methylvinylsilane, or bis(di-n-butylamino) methylvinylsilane.

The amount of the silicon-containing vinyl compound used in production of the conjugated diene polymer is preferably not less than 0.01% by mass, more preferably not less than 0.02% by mass, and still more preferably not less than 0.05% by mass based on 100% by mass of the total amount of the monomer component used in the polymerization for achieving a balanced enhancement in processability, fuel economy, rubber strength, abrasion resistance, wet-grip performance, and handling stability. The amount is preferably not more than 20% by mass, more preferably not more than 2% by mass, and still more preferably not more than 1% by mass for achieving better cost efficiency and higher rubber strength.

In the production of the conjugated diene polymer, the monomer component may further include polymerizable monomers in addition to the conjugated diene compound and silicon-containing vinyl compound. The monomers may be, for example, aromatic vinyl compounds, vinyl nitriles, and unsaturated carboxylic acid esters. Examples of the aromatic vinyl compounds include styrene, α-methylstyrene, vinyltoluene, vinylnaphthalene, divinylbenzene, trivinylbenzene, and divinylnaphthalene. Examples of the vinyl nitriles include acrylonitrile. Examples of the unsaturated carboxylic acid esters include methyl acrylate, ethyl acrylate, methyl methacrylate, and ethyl methacrylate. Aromatic vinyl compounds are preferable, and styrene is more preferable among the above examples.

In the case where an aromatic vinyl compound is used in the production of the conjugated diene polymer, the amount of the aromatic vinyl compound based on 100% by mass of the combined amount of the conjugated diene compound and the aromatic vinyl compound is preferably not less than 10% by mass (the amount of the conjugated diene compound is not more than 90% by mass), and more preferably not less than 15% by mass (the amount of the conjugated diene compound is not more than 85% by mass). Moreover, from a viewpoint of fuel economy, the amount of the aromatic vinyl compound is preferably not more than 50% by mass (the amount of the conjugated diene compound is not less than 50% by mass), and more preferably not more than 45% by mass (the amount of the conjugated diene compound is not less than 55% by mass).

In the production of the conjugated diene polymer, polymerization is preferably performed in a hydrocarbon solvent that does not inactivate the polymerization initiator represented by the formula (I). Examples of the hydrocarbon solvent include aliphatic hydrocarbons, aromatic hydrocarbons, and alicyclic hydrocarbons. Examples of the aliphatic hydrocarbons include propane, n-butane, iso-butane, n-pentane, iso-pentane, n-hexane, n-heptane, and n-octane. Examples of the aromatic hydrocarbons include benzene, toluene, xylene, and ethylbenzene. Examples of the alicyclic hydrocarbons include cyclopentane and cyclohexane. The hydrocarbon solvent may be a mixture of various components, such as industrial hexane. It is preferably a C_2-12 hydrocarbon.

The polymerization reaction may be performed in the presence of an agent for adjusting the vinyl bond content in a conjugated diene unit, or an agent for adjusting distribution of a conjugated diene unit and a monomer unit based on a monomer other than conjugated diene in a conjugated diene-based polymer chain (hereinafter, collectively referred to as “adjusting agent”). Examples of the agents include ether compounds, tertiary amine compounds, and phosphine compounds. Examples of the ether compounds include cyclic ethers such as tetrahydrofuran, tetrahydropyran, and 1,4-dioxane; aliphatic monoethers such as diethyl ether and dibutyl ether; aliphatic diethers such as ethylene glycol dimethyl ether, ethylene glycol diethyl ether, ethylene glycol dibutyl ether, diethylene glycol diethyl ether, and diethylene glycol dibutyl ether; and aromatic ethers such as diphenyl ether and anisole. Examples of the tertiary amine compounds include triethylamine, tripropylamine, tributylamine, N,N,N′,N′-tetramethylethylenediamine, N,N-diethylaniline, pyridine, and quinoline. Examples of the phosphine compounds include trimethylphosphine, triethylphosphine, and triphenylphosphine. One or more of them are used.

In the production of the conjugated diene polymer, the polymerization initiator may be supplied to a polymerization reactor before the monomer component is supplied to the polymerization reactor; or the polymerization initiator may be supplied to the polymerization reactor after the whole amount of the monomer component used in polymerization is supplied to the polymerization reactor; or the polymerization initiator may be supplied to the polymerization reactor after a part of the monomer component used in polymerization is supplied to the polymerization reactor. The polymerization initiator may be supplied at once or continuously to the polymerization reactor.

In the production of the conjugated diene polymer, the monomer component may be supplied at once, continuously, or intermittently to the polymerization reactor. Moreover, respective monomers may be supplied separately, or simultaneously to the polymerization reactor.

In the production of the conjugated diene polymer, the polymerization temperature is usually 25 to 100° C., preferably 35 to 90° C., and more preferably 50 to 80° C. The polymerization time is usually 10 minutes to 5 hours.

The conjugated diene polymer is obtained by polymerizing a monomer component including a conjugated diene compound and a silicon-containing vinyl compound in the presence of a polymerization initiator represented by the formula (I) to produce a copolymer, and then reacting a compound containing a nitrogen atom and/or a silicon atom with an active terminal of the copolymer (the active terminal of the copolymer is considered to have an alkali metal derived from the polymerization initiator) (terminal modification reaction). Specifically, the conjugated diene polymer is obtained by adding a compound containing a nitrogen atom and/or a silicon atom to a polymerization solution and then mixing them. The amount of the compound containing a nitrogen atom and/or a silicon atom to be added to the polymerization solution is usually 0.1 to 3 mol, preferably 0.5 to 2 mol, and more preferably 0.7 to 1.5 mol, per mol of an alkali metal derived from the polymerization initiator represented by the formula (I).

The terminal modification reaction is performed usually at a temperature from 25 to 100° C., preferably from 35 to 90° C., and more preferably from 50 to 80° C. The time period for the reaction is usually 60 seconds to 5 hours, preferably 5 minutes to 1 hour, and more preferably 15 minutes to 1 hour.

Preferable examples of the compound containing a nitrogen atom and/or a silicon atom include a compound containing a nitrogen atom and a carbonyl group.

The compound containing a nitrogen atom and a carbonyl group is preferably a compound represented by the following formula (III):

##STR00011##
wherein R³¹ represents an optionally substituted hydrocarbyl group, or is bonded with R³² to form a hydrocarbylene group optionally containing, as a hetero atom, a nitrogen atom and/or an oxygen atom, or is bonded with R³⁴ to form a divalent group; R³² represents an optionally substituted hydrocarbyl group, or is bonded with R³¹ to form a hydrocarbylene group optionally containing, as a hetero atom, a nitrogen atom and/or an oxygen atom; and R³⁴ represents an optionally substituted hydrocarbyl group, or a hydrogen atom, or is bonded with Rn to form a divalent group; R³³ represents a divalent group; and k represents 0 or 1.

In the formula (III), the optionally substituted hydrocarbyl group in R³¹, R³² or R³⁴ is a hydrocarbyl group or a substituted hydrocarbyl group. Examples of the substituted hydrocarbyl group include a substituted hydrocarbyl group in which the substituent is a hydrocarbyloxy group, and a substituted hydrocarbyl group in which the substituent is a substituted amino group. Examples of the hydrocarbyl group include alkyl groups such as a methyl group, an ethyl group, an n-propyl group, an isopropyl group, and an n-butyl group; alkenyl groups such as a vinyl group, an allyl group, and an isopropenyl group; and aryl groups such as a phenyl group. Examples of the substituted hydrocarbyl group in which the substituent is a hydrocarbyloxy group include alkoxyalkyl groups such as a methoxymethyl group, an ethoxymethyl group, and an ethoxyethyl group. Examples of the substituted hydrocarbyl group in which the substituent is a substituted amino group include (N,N-dialkylamino)alkyl groups such as a 2-(N,N-dimethylamino) ethyl group, a 2-(N,N-diethylamino)ethyl group, a 3-(N,N-dimethylamino)propyl group, and a 3-(N,N-diethylamino)propyl group; (N,N-dialkylamino)aryl groups such as a 4-(N,N-dimethylamino)phenyl group, a 3-(N,N-dimethylamino)phenyl group, a 4-(N,N-diethylamino)phenyl group, and a 3-(N,N-diethylamino)phenyl group; (N,N-dialkylamino)alkylaryl groups such as a 4-(N,N-dimethylamino)methylphenyl group and a 4-(N,N-dimethylamino)ethylphenyl group; cyclic amino group-containing alkyl groups such as a 3-pyrrolidinopropyl group, a 3-piperidinopropyl group, and a 3-imidazolylpropyl group; cyclic amino group-containing aryl groups such as a 4-pyrrolidinophenyl group, a 4-piperidinophenyl group, and a 4-imidazolylphenyl group; and cyclic amino group-containing alkylaryl groups such as a 4-pyrrolidinoethylphenyl group, a 4-piperidinoethylphenyl group, and a 4-imidazolylethylphenyl group.

In the formula (III), the hydrocarbylene group optionally containing, as a hetero atom, a nitrogen atom and/or an oxygen atom, formed by bonding of R³¹ and R³², is a hydrocarbylene group or a hetero atom-containing hydrocarbylene group in which the hetero atom is a nitrogen atom and/or an oxygen atom. Examples of the hetero atom-containing hydrocarbylene group in which the hetero atom is a nitrogen atom and/or an oxygen atom include a hetero atom-containing hydrocarbylene group in which the hetero atom is a nitrogen atom and a hetero atom-containing hydrocarbylene group in which the hetero atom is an oxygen atom. Examples of the hydrocarbylene group include alkylene groups such as a trimethylene group, a tetramethylene group, a pentamethylene group, a hexamethylene group, a pentan-2-en-1,5-diyl group, and a 2,2,4-trimethylhexane-1,6-diyl group; and arylene groups such as a 1,4-phenylene group. Examples of the hetero atom-containing hydrocarbylene group in which the hetero atom is a nitrogen atom include a group represented by —CH═N—CH═CH— and a group represented by —CH═N—CH₂—CH₂—. Examples of the hetero atom-containing hydrocarbylene group in which the hetero atom is an oxygen atom include a group represented by —(CH₂)_s—O—(CH₂)_t— (s and t each are an integer of 1 or more).

In the formula (III), examples of the divalent group formed by bonding of R³¹ and R³⁴, and the divalent group of R³³ include a hydrocarbylene group, a hetero atom-containing hydrocarbylene group in which the hetero atom is a nitrogen atom, a hetero atom-containing hydrocarbylene group in which the hetero atom is an oxygen atom, a group in which a hydrocarbylene group and an oxygen atom are bonded, and a group in which a hydrocarbylene group and a group represented by —NR³⁵— (R³⁵ represents a hydrocarbyl group or a hydrogen atom) are bonded. Examples of the hydrocarbylene group include alkylene groups such as a trimethylene group, a tetramethylene group, a pentamethylene group, a hexamethylene group, a pentan-2-en-1,5-diyl group, and a 2,2,4-trimethylhexane-1,6-diyl group; and arylene groups such as a 1,4-phenylene group. Examples of the hetero atom-containing hydrocarbylene group in which the hetero atom is a nitrogen atom include a group represented by —CH═N—CH═CH— and a group represented by —CH═N—CH₂—CH₂—. Examples of the hetero atom-containing hydrocarbylene group in which the hetero atom is an oxygen atom include a group represented by —(CH₂)_s—O—(CH₂)_t— (s and t each are an integer of 1 or more). Examples of the group in which a hydrocarbylene group and an oxygen atom are bonded include a group represented by —(CH₂)_r—O— (r represents an integer of 1 or more). Examples of the group in which a hydrocarbylene group and a group represented by —NR³⁵— (R³⁵ represents a hydrocarbyl group or a hydrogen atom) are bonded include a group represented by —(CH₂)_p—NR³⁵— (R³⁵ represents a hydrocarbyl group (preferably a C_1-6 hydrocarbyl group), or a hydrogen atom; and p represents an integer of 1 or more).

Preferable examples of a compound represented by the formula (III) include a compound represented by the formula (III) in which k is 0, and R³⁴ is an optionally substituted hydrocarbyl group or a hydrogen atom, represented by the following formula (IIIa):

##STR00012##
wherein, R³¹ represents an optionally substituted hydrocarbyl group, or is bonded with R³² to form a hydrocarbylene group optionally containing, as a hetero atom, a nitrogen atom and/or an oxygen atom; R³² represents an optionally substituted hydrocarbyl group, or is bonded with R³¹ to form a hydrocarbylene group optionally containing, as a hetero atom, a nitrogen atom and/or an oxygen atom; and R³⁴ represents an optionally substituted hydrocarbyl group or a hydrogen atom.

In the formula (IIIa), description and examples of the optionally substituted hydrocarbyl group for R³¹, R³² or R³⁴, and the hydrocarbylene group optionally containing, as a hetero atom, a nitrogen atom and/or an oxygen atom, formed by bonding of R³¹ and R³², are the same as those stated in the description of the formula (III).

In the formula (IIIa), R³¹ is preferably a C_1-10 hydrocarbyl group, or is bonded with R³² to form a C_3-10 hydrocarbylene group or a hetero atom-containing C_3-10 hydrocarbylene group in which the hetero atom is a nitrogen atom. R³¹ is more preferably a C_1-10 alkyl group or a C_6-10 aryl group, or is bonded with R³² to form a C_3-10 alkylene group, a group represented by —CH═N—CH═CH—, or a group represented by —CH═N—CH₂—CH₂—. R³¹ is still more preferably a C_1-6 alkyl group, and particularly preferably a methyl group or an ethyl group.

In the formula (IIIa), R³² is preferably a C_1-10 hydrocarbyl group, or is bonded with R³¹ to form a C_3-10 hydrocarbylene group or a hetero atom-containing C_3-10 hydrocarbylene group in which the hetero atom is a nitrogen atom. R³² is more preferably a C_1-10 alkyl group or a C_6-10 aryl group, or is bonded with R³¹ to form a C_3-10 alkylene group, a group represented by —CH═N—CH═CH—, or a group represented by —CH═N—CH₂—CH₂—. R³² is still more preferably a C_1-6 alkyl group, and particularly preferably a methyl group or an ethyl group.

In the formula (IIIa), R³⁴ is preferably a hydrocarbyl group or a hydrogen atom, more preferably a C_1-10 hydrocarbyl group or a hydrogen atom, still more preferably a C_1-6 alkyl group or a hydrogen atom, and particularly preferably a hydrogen atom, a methyl group or an ethyl group.

Examples of the compound represented by the formula (IIIa) in which R³⁴ is a hydrocarbyl group include N,N-dihydrocarbylacetamides such as N,N-dimethylacetamide, N,N-diethylacetamide, and N-methyl-N-ethylacetamide; N,N-dihydrocarbylacrylamides such as N,N-dimethylacrylamide, N,N-diethylacrylamide, and N-methyl-N-ethylacrylamide; and N,N-dihydrocarbylmethacrylamides such as N,N-dimethylmethacrylamide, N,N-diethylmethacrylamide, and N-methyl-N-ethylmethacrylamide.

Examples of the compound represented by the formula (IIIa) in which R³⁴ is a hydrogen atom include N,N-dihydrocarbylformamides such as N,N-dimethylformamide, N,N-dimethylformamide, and N-methyl-N-ethylformamide.

Preferable examples of the compound represented by the formula (III) include a compound represented by the formula (III) in which k is 0; and R³⁴ is bonded with R³¹ to form a divalent group, represented by the following formula (IIIb):

##STR00013##
wherein R³² represents an optionally substituted hydrocarbyl group; and R³⁶ represents a hydrocarbylene group, or a group in which a hydrocarbylene group and a group represented by —NR³⁵— are bonded, where R³⁵ represents a hydrocarbyl group or a hydrogen atom.

In the formula (IIIb), description and examples of an optionally substituted hydrocarbyl group for R³² are the same as those stated in the description of the formula (III).

In the formula (IIIb), examples of the hydrocarbylene group for R³⁶ include alkylene groups such as a trimethylene group, a tetramethylene group, a pentamethylene group, a hexamethylene group, a pentan-2-en-1,5-diyl group, and a 2,2,4-trimethylhexane-1,6-diyl group; and arylene groups such as a 1,4-phenylene group. Examples of the group in which a hydrocarbylene group and a group represented by —NR³⁵— (R³⁵ represents a hydrocarbyl group or a hydrogen atom) are bonded for R³⁶ include a group represented by —(CH₂)_p—NR³⁵— (R³⁵ represents a hydrocarbyl group or a hydrogen atom, and p represents an integer of 1 or more).

In the formula (IIIb), R³² is preferably a C_1-10 hydrocarbyl group, more preferably a C_1-10 alkyl group or a C_6-10 aryl group, still more preferably a C_1-6 alkyl group or a phenyl group, and particularly preferably a methyl group, an ethyl group, or a phenyl group.

In the formula (IIIb), R³⁶ is preferably a C_1-10 hydrocarbylene group, or a group in which a C_1-10 hydrocarbylene group and a group represented by —NR³⁵— (R³⁵ represents a hydrocarbyl group (preferably a C_1-10 hydrocarbyl group) or a hydrogen atom) are bonded, more preferably a C_3-6 alkylene group or a group represented by —(CH₂)_p—NR³⁵— (R³⁵ represents a hydrocarbyl group (preferably a C_1-10 hydrocarbyl group), and p represents an integer of not less than 1 (preferably an integer of 2 to 5)), and further preferably a trimethylene group, a tetramethylene group, a pentamethylene group, or a group represented by —(CH₂)₂—N(CH₃)—.

Examples of the compound represented by the formula (IIIb) in which R³⁶ is a hydrocarbylene group include N-hydrocarbyl-β-propiolactams such as N-methyl-β-propiolactam and N-phenyl-β-propiolactam; N-hydrocarbyl-2-pyrrolidones such as N-methyl-2-pyrrolidone, N-vinyl-2-pyrrolidone, N-phenyl-2-pyrrolidone, N-tert-butyl-2-pyrrolidone, and N-methyl-5-methyl-2-pyrrolidone; N-hydrocarbyl-2-piperidones such as N-methyl-2-piperidone, N-vinyl-2-piperidone, and N-phenyl-2-piperidone; N-hydrocarbyl-ε-caprolactams such as N-methyl-ε-caprolactam and N-phenyl-ε-caprolactam; and N-hydrocarbyl-ω-laurilolactams such as N-methyl-ω-laurilolactam and N-vinyl-ω-laurilolactam. N-phenyl-2-pyrrolidone and N-methyl-ε-caprolactam are preferable among the above examples.

Examples of the compound represented by the formula (IIIb) in which R³⁶ is a group in which a hydrocarbylene group and a group represented by —NR³⁵— (R³⁵ is a hydrocarbyl group or a hydrogen atom) are bonded include 1,3-dihydrocarbyl-2-imidazolidinones such as 1,3-dimethyl-2-imidazolidinone, 1,3-diethyl-2-imidazolidinone, 1,3-divinyl-2-imidazolidinone, and 1-methyl-3-ethyl-2-imidazolidinone. Among the above examples, 1,3-dimethyl-2-imidazolidinone is preferred.

Preferable examples of the compound represented by the formula (III) include a compound represented by the formula (III) in which k is 1; and R³³ is a hydrocarbylene group, represented by the following formula (IIIc):

##STR00014##
wherein R³¹ represents an optionally substituted hydrocarbyl group, or is bonded with R³² to form a hydrocarbylene group optionally containing, as a hetero atom, a nitrogen atom and/or an oxygen atom; R³² represents an optionally substituted hydrocarbyl group, or is bonded with R³¹ to form a hydrocarbylene group optionally containing, as a hetero atom, a nitrogen atom and/or an oxygen atom; R³³ represents a hydrocarbylene group, and R³⁴ represents an optionally substituted hydrocarbyl group or a hydrogen atom.

In the formula (IIIc), description and examples of the optionally substituted hydrocarbyl group for R³¹, R³² or R³⁴; the hydrocarbylene group optionally containing, as a hetero atom, a nitrogen atom and/or an oxygen atom, formed by bonding of R³¹ and R³²; and the hydrocarbylene group for R³³ are the same as those stated in the description of the formula (III).

In the formula (IIIc), R³³ is preferably a C_1-10 hydrocarbylene group, more preferably a C_1-10 alkylene group or a C_6-10 arylene group, still more preferably a C_1-6 alkylene group or a phenylene group, and particularly preferably an ethylene group, a trimethylene group, or a 1,4-phenylene group.

In the formula (IIIc), R³⁴ is preferably a C_1-10 hydrocarbyl group, or a substituted C_1-10 hydrocarbyl group in which the substituent is a dialkylamino group, more preferably a C_1-6 alkyl group, a C_6-10 aryl group, a C_1-6 dialkylaminoalkyl group, or a C_6-10 dialkylaminoaryl group, and still more preferably a methyl group, an ethyl group, a phenyl group, a 3-dimethylaminoethyl group, or a 4-diethylaminophenyl group.

In the formula (IIIc), R³¹ is preferably a C_1-10 hydrocarbyl group, or is bonded with R³² to form a C_3-10 hydrocarbylene group, or a hetero atom-containing C_3-10 hydrocarbylene group in which the hetero atom is a nitrogen atom or an oxygen atom; more preferably a C_1-10 alkyl group or a C_6-10 aryl group, or is bonded with R³² to form a C_3-10 alkylene group, a group represented by —CH═N—CH═CH—, a group represented by —CH═N—CH₂—CH₂—, or a group represented by —(CH₂)₂—O—(CH₂)₂—; still more preferably a C_1-6 alkyl group, or is bonded with R³² to form a C_3-6 alkylene group, a group represented by —CH═N—CH═CH—, or a group represented by —CH═N—CH₂—CH₂—; and particularly preferably a methyl group or an ethyl group, or is bonded with R³² to form a tetramethylene group, a hexamethylene group, or a group represented by —CH═N—CH═CH—.

In the formula (IIIc), R³² is preferably a C_1-10 hydrocarbyl group, or is bonded with R³¹ to form a C_3-10 hydrocarbylene group, or a hetero atom-containing C_3-10 hydrocarbylene group in which the hetero atom is a nitrogen atom or an oxygen atom; more preferably a C_1-10 alkyl group or a C_6-10 aryl group, or is bonded with R³¹ to form a C_3-10 alkylene group, a group represented by —CH═N—CH═CH—, a group represented by —CH═N—CH₂—CH₂—, or a group represented by —(CH₂)₂—O—(CH₂)₂—; still more preferably a C_1-6 alkyl group, or is bonded with R³¹ to form a C_3-6 alkylene group, a group represented by —CH═N—CH═CH—, or a group represented by —CH═N—CH₂—CH₂—; and particularly preferably a methyl group or an ethyl group, or is bonded with R³¹ to form a tetramethylene group, a hexamethylene group, or a group represented by —CH═N—CH═CH—.

Examples of the compound represented by the formula (IIIc) in which R³⁴ is a hydrocarbyl group include 4-N,N-dihydrocarbylaminoacetophenones such as 4-(N,N-dimethylamino)acetophenone, 4-N-methyl-N-ethylaminoacetophenone, and 4-N,N-diethylaminoacetophenone; and 4-cyclic aminoacetophenone compounds such as 4′-(imidazol-1-yl)acetophenone and 4-pyrazolylacetophenone. Among the above examples, a 4-cyclic aminoacetophenone compound is preferable, and 4′-(imidazol-1-yl)acetophenone is more preferable.

Examples of the compound represented by the formula (IIIc) in which R³⁴ is a substituted hydrocarbyl group include bis(dihydrocarbylaminoalkyl)ketones such as 1,7-bis(methylethylamino)-4-heptanone and 1,3-bis(diphenylamino)-2-propanone; 4-(dihydrocarbylamino)benzophenones such as 4-N,N-dimethylaminobenzophenone, 4-N,N-di-t-butylaminobenzophenone, and 4-N,N-diphenylaminobenzophenone; and 4,4′-bis(dihydrocarbylamino)benzophenones such as 4,4′-bis(dimethylamino)benzophenone, 4,4′-bis(diethylamino)benzophenone, and 4,4′-bis(diphenylamino)benzophenone. Among the above examples, 4,4′-bis(dihydrocarbylamino)benzophenone is preferable, and 4,4′-bis(diethylamino)benzophenone is more preferable.

Preferable examples of the compound represented by the formula (III) include a compound represented by the formula (III) in which k is 1, and R³³ is a group in which a hydrocarbylene group and an oxygen atom are bonded, or a group in which a hydrocarbylene group and a group represented by —NR³⁵— (R³⁵ represents a hydrocarbyl group or a hydrogen atom) are bonded, represented by the following formula (IIId):

##STR00015##
wherein R³¹ represents an optionally substituted hydrocarbyl group, or is bonded with R³² to form a hydrocarbylene group optionally containing, as a hetero atom, a nitrogen atom and/or an oxygen atom; R³² represents an optionally substituted hydrocarbyl group, or is bonded with R³¹ to form a hydrocarbylene group optionally containing, as a hetero atom, a nitrogen atom and/or an oxygen atom; R³⁷ represents a hydrocarbylene group; A represents an oxygen atom or —NR³⁵— wherein R³⁵ represents a hydrocarbyl group or a hydrogen atom; and R³⁴ represents an optionally substituted hydrocarbyl group or a hydrogen atom.

In the formula (IIId), description and examples of the optionally substituted hydrocarbyl group for R³¹, R³² or R³⁴, and the hydrocarbylene group optionally containing, as a hetero atom, a nitrogen atom and/or an oxygen atom, formed by bonding of R³¹ and R³², are the same as those stated in the description of the formula (III). The hydrocarbyl group for R³⁵ is the same as the hydrocarbyl group for R³¹, R³², or R³⁴.

In the formula (IIId), A is preferably an oxygen atom or a group represented by —NR³⁵— (R³⁵ is a hydrocarbyl group (preferably a C_1-5 hydrocarbyl group) or a hydrogen atom), more preferably an oxygen atom or a group represented by —NH—, and still more preferably a group represented by —NH—.

In the formula (IIId), examples of the hydrocarbylene group for R³⁷ include alkylene groups such as a trimethylene group, a tetramethylene group, a pentamethylene group, a hexamethylene group, a pentan-2-en-1,5-diyl group, and a 2,2,4-trimethylhexane-1,6-diyl group; and arylene groups such as a 1,4-phenylene group.

In the formula (IIId), R³⁴ is preferably a C_1-10 hydrocarbyl group, more preferably an alkenyl group having 2 to 5 carbon atoms, and still more preferably a vinyl group.

In the formula (IIId), R³⁷ is preferably a C_1-10 hydrocarbylene group, more preferably a C_1-6 alkylene group, still more preferably an ethylene group or a trimethylene group, and particularly preferably a trimethylene group.

In the formula (IIId), R³¹ is preferably a C_1-10 hydrocarbyl group, or is bonded with R³² to form a C_3-10 hydrocarbylene group, or a hetero atom-containing C_3-10 hydrocarbylene group in which the hetero atom is a nitrogen atom or an oxygen atom; more preferably a C_1-10 alkyl group alkylene group, a group represented by —CH═N—CH═CH—, a group represented by —CH═N—CH₂—CH₂—, or a group represented by —(CH₂)₂—O—(CH₂)₂—; still more preferably a C_1-6 alkyl group, or is bonded with R³² to form a C_3-6 alkylene group, a group represented by —CH═N—CH═CH—, or a group represented by —CH═N—CH₂—CH₂—; and particularly preferably a methyl group or an ethyl group, or is bonded with R³² to form a tetramethylene group, a hexamethylene group, or a group represented by —CH═N—CH═CH—.

In the formula (IIId), R³² is preferably a C_1-10 hydrocarbyl group, or is bonded with Rn to form a C_3-10 hydrocarbylene group, or a hetero atom-containing C_3-10 hydrocarbylene group in which the hetero atom is a nitrogen atom or an oxygen atom; more preferably a C_1-10 alkyl group or a C_6-10 aryl group, or is bonded with R³¹ to form a C_3-10 alkylene group, a group represented by —CH═N—CH═CH—, a group represented by —CH═N—CH₂—CH₂—, or a group represented by —(CH₂)₂—O—(CH₂)₂—; still more preferably a C_1-6 alkyl group, or is bonded with R³¹ to form a C_3-6 alkylene group, a group represented by —CH═N—CH═CH—, or a group represented by —CH═N—CH₂—CH₂—; and particularly preferably a methyl group or an ethyl group, or is bonded with R³¹ to form a tetramethylene group, a hexamethylene group, or a group represented by —CH═N—CH═CH—.

Examples of the compound represented by the formula (IIId) in which A is an oxygen atom include 2-N,N-dihydrocarbylaminoethyl acrylates such as 2-N,N-dimethylaminoethyl acrylate and 2-N,N-diethylaminoethyl acrylate; 3-N,N-dihydrocarbylaminopropyl acrylates such as 3-N,N-dimethylaminopropyl acrylate; 2-N,N-dihydrocarbylaminoethyl methacrylates such as 2-N,N-dimethylaminoethyl methacrylate and 2-N,N-diethylaminoethyl methacrylate; and 3-N,N-dihydrocarbylaminopropyl methacrylates such as 3-N,N-dimethylaminopropyl methacrylate. The compound is preferably 3-N,N-dihydrocarbylaminopropyl acrylate, and more preferably 3-N,N-dimethylaminopropyl acrylate.

Examples of the compound represented by the formula (IIId) in which A is a group represented by —NR³⁵— (R³⁵ is a hydrocarbyl group or a hydrogen atom) include N,N-dihydrocarbylaminoethylacrylamides such as N,N-dimethylaminoethylacrylamide and N,N-diethylaminoethylacrylamide; N,N-dihydrocarbylaminopropylacrylamides such as N,N-dimethylaminopropylacrylamide and N,N-diethylaminopropylacrylamide; N,N-dihydrocarbylaminobutylacrylamides such as N,N-dimethylaminobutylacrylamide and N,N-diethylaminobutylacrylamide; N,N-dihydrocarbylaminoethylmethacrylamides such as N,N-dimethylaminoethylmethacrylamide and N,N-diethylaminoethylmethacrylamide; N,N-dihydrocarbylaminopropylmethacrylamides such as N,N-dimethylaminopropylmethacrylamide and N,N-diethylaminopropylmethacrylamide; and N,N-dihydrocarbylaminobutylmethacrylamides such as N,N-dimethylaminobutylmethacrylamide and N,N-diethylaminobutylmethacrylamide. The compound is preferably N,N-dihydrocarbylaminopropylacrylamide, and more preferably N,N-dimethylaminopropylacrylamide.

The compound represented by the formula (III) is preferably a compound represented by the formula (IIId), particularly preferably N,N-dihydrocarbylaminopropylacrylamide, and most preferably N,N-dimethylaminopropylacrylamide.

In addition to those described above, preferable examples of the compound containing a nitrogen atom and/or a silicon atom include an alkoxysilyl group-containing compound.

The alkoxysilyl group-containing compound is preferably a compound containing a nitrogen atom and an alkoxysilyl group, and more preferably a compound represented by the following formula (IV):

##STR00016##
wherein R⁴¹ represents a hydrocarbyl group; R⁴² and R⁴³ each represent a hydrocarbyl group or a hydrocarbyloxy group; R⁴⁴ represents an optionally substituted hydrocarbyl group or a trihydrocarbylsilyl group, or is bonded with R⁴⁵ to form a hydrocarbylene group optionally containing, as a hetero atom, at least one selected from the group consisting of a silicon atom, a nitrogen atom and an oxygen atom; R⁴⁵ represents an optionally substituted hydrocarbyl group or a trihydrocarbylsilyl group, or is bonded with R⁴⁴ to form a hydrocarbylene group optionally containing, as a hetero atom, at least one selected from the group consisting of a silicon atom, a nitrogen atom and an oxygen atom; and j represents an integer of 1 to 5.

In the formula (IV), the optionally substituted hydrocarbyl group is a hydrocarbyl group or a substituted hydrocarbyl group. Examples of the hydrocarbyl group include alkyl groups such as a methyl group, an ethyl group, an n-propyl group, an isopropyl group, and an n-butyl group; alkenyl groups such as a vinyl group, an allyl group, and an isopropenyl group; and aryl groups such as a phenyl group. The hydrocarbyl group is preferably an alkyl group, and more preferably a methyl group or an ethyl group. Examples of the substituted hydrocarbyl group include oxacycloalkyl groups such as an oxiranyl group and a tetrahydrofuranyl group, and preferably a tetrahydrofuranyl group.

Herein, the oxacycloalkyl group represents a group in which CH₂ on an alicycle of a cycloalkyl group is replaced with an oxygen atom.

Examples of the hydrocarbyloxy group include alkoxy groups such as a methoxy group, an ethoxy group, an n-propoxy group, an isopropoxy group, an n-butoxy group, a sec-butoxy group, and a tert-butoxy group; and aryloxy groups such as a phenoxy group and a benzyloxy group. The hydrocarbyloxy group is preferably an alkoxy group, and more preferably a methoxy group or an ethoxy group.

Examples of the trihydrocarbylsilyl group include a trimethylsilyl group and a tert-butyl-dimethylsilyl group, and preferably a trimethylsilyl group.

The hydrocarbylene group optionally containing, as a hetero atom, at least one selected from the group consisting of a silicon atom, a nitrogen atom and an oxygen atom is a hydrocarbylene group, or a hetero atom-containing hydrocarbylene group in which the hetero atom is at least one selected from the group consisting of a silicon atom, a nitrogen atom and an oxygen atom. Examples of the hetero atom-containing hydrocarbylene group in which the hetero atom is at least one selected from the group consisting of a silicon atom, a nitrogen atom and an oxygen atom include a hetero atom-containing hydrocarbylene group in which the hetero atom is a silicon atom, a hetero atom-containing hydrocarbylene group in which the hetero atom is a nitrogen atom, and a hetero atom-containing hydrocarbylene group in which the hetero atom is an oxygen atom. Examples of the hydrocarbylene group include alkylene groups such as a tetramethylene group, a pentamethylene group, a hexamethylene group, a pentan-2-en-1,5-diyl group, and a 2,2,4-trimethylhexane-1,6-diyl group. Among them, a C_4-7 alkylene group is preferable, and a pentamethylene group or a hexamethylene group is more preferable. Examples of the hetero atom-containing hydrocarbylene group in which the hetero atom is a silicon atom include a group represented by —Si(CH₃)₂—CH₂—CH₂—Si(CH₃)₂—. Examples of the hetero atom-containing hydrocarbylene group in which the hetero atom is a nitrogen atom include a group represented by —CH═N—CH═CH—, or a group represented by —CH═N—CH₂—CH₂—. Examples of the hetero atom-containing hydrocarbylene group in which the hetero atom is an oxygen atom include a group represented by —CH₂—CH₂—O—CH₂—CH₂—.

In the formula (IV), R⁴¹ is preferably a C_1-4 alkyl group, and more preferably a methyl group or an ethyl group. R⁴² and R⁴³ each are preferably a hydrocarbyloxy group, more preferably a C_1-4 alkoxy group, and still more preferably a methoxy group or an ethoxy group. R⁴⁴ and R⁴⁵ each are preferably a hydrocarbyl group, more preferably a C_1-4 alkyl group, and still more preferably a methyl group or an ethyl group. Here, j is preferably an integer of 2 to 4.

Examples of the compound represented by the formula (IV) include [(dialkylamino)alkyl]alkoxysilane compounds such as 3-dimethylaminopropyltriethoxysilane, 3-dimethylaminopropyltrimethoxysilane, 3-diethylaminopropyltriethoxysilane, 3-diethylaminopropyltrimethoxysilane, 3-dimethylaminopropylmethyldiethoxysilane, 2-dimethylaminoethyltriethoxysilane, and 2-dimethylaminoethyltrimethoxysilane; cyclic aminoalkylalkoxysilane compounds such as hexamethyleneiminomethyltrimethoxysilane, 3-hexamethyleneiminopropyltriethoxysilane, N-(3-triethoxysilylpropyl)-4,5-dihydroimidazole, and N-(3-trimethoxysilylpropyl)-4,5-imidazole; [di(tetrahydrofuranyl)amino]alkylalkoxysilane compounds such as 3-[di(tetrahydrofuranyl)amino]propyltrimethoxysilane and 3-[di(tetrahydrofuranyl)amino]propyltriethoxysilane; and N,N-bis(trialkylsilyl)aminoalkylalkoxysilane compounds such as N,N-bis(trimethylsilyl)aminopropylmethyldimethoxysilane and N,N-bis(trimethylsilyl)aminopropylmethyldiethoxysilane. Among the above examples, [(dialkylamino)alkyl]alkoxysilane compounds are preferable, and 3-dimethylaminopropyltriethoxysilane, 3-dimethylaminopropyltrimethoxysilane, 3-diethylaminopropyltriethoxysilane, and 3-diethylaminopropyltrimethoxysilane are more preferable.

Examples of the compound containing an alkoxysilyl group, in addition to the aforementioned compounds containing a nitrogen atom and an alkoxysilyl group, include tetraalkoxysilanes such as tetramethoxysilane, tetraethoxysilane, and tetra-n-propoxysilane; trialkoxyhydrocarbylsilanes such as methyltrimethoxysilane, methyltriethoxysilane, ethyltrimethoxysilane, and phenyltrimethoxysilane; trialkoxyhalosilanes such as trimethoxychlorosilane, triethoxychlorosilane, and tri-n-propoxychlorosilane; dialkoxydihydrocarbylsilanes such as dimethoxydimethylsilane, diethoxydimethylsilane, and dimethoxydiethylsilane; dialkoxydihalosilanes such as dimethoxydichlorosilane, diethoxydichlorosilane, and di-n-propoxydichlorosilane; monoalkoxytrihydrocarbylsilanes such as methoxytrimethylsilane; monoalkoxytrihalosilanes such as methoxytrichlorosilane and ethoxytrichlorosilane; (glycidoxyalkyl)alkoxysilane compounds such as 2-glycidoxyethyltrimethoxysilane, 2-glycidoxyethyltriethoxysilane, (2-glycidoxyethyl)methyldimethoxysilane, 3-glycidoxypropyltrimethoxysilane, 3-glycidoxypropyltriethoxysilane, and (3-glycidoxypropyl)methyldimethoxysilane; (3,4-epoxycyclohexyl)alkylalkoxysilane compounds such as 2-(3,4-epoxycyclohexyl)ethyltrimethoxysilane, 2-(3,4-epoxycyclohexyl)ethyltriethoxysilane, and 2-(3,4-epoxycyclohexyl)ethyl(methyl)dimethoxysilane; alkoxysilylalkylsuccinic acid anhydrides such as 3-trimethoxysilylpropylsuccinic acid anhydride and 3-triethoxysilylpropylsuccinic acid anhydride; and (methacryloyloxyalkyl)alkoxysilane compounds such as 3-methacryloyloxypropyltrimethoxysilane and 3-methacryloyloxypropyltriethoxysilane.

The compound containing an alkoxysilyl group may contain a nitrogen atom and a carbonyl group. Examples of the compound containing a nitrogen atom and a carbonyl group as well as an alkoxysilyl group include tris[(alkoxysilyl)alkyl]isocyanurate compounds such as tris[3-(trimethoxysilyl)propyl]isocyanurate, tris[3-(triethoxysilyl)propyl]isocyanurate, tris[3-(tripropoxysilyl)propyl]isocyanurate, and tris[3-(tributoxysilyl)propyl]isocyanurate. Among them, tris[3-(trimethoxysilyl)propyl]isocyanurate is preferable.

Examples of the compound containing a nitrogen atom and/or a silicon atom include an N,N-dialkyl-substituted carboxylic acid amide dialkyl acetal compound. Examples of the N,N-dialkyl-substituted carboxylic acid amide dialkyl acetal compound include N,N-dialkylformamide dialkyl acetals such as N,N-dimethylformamide dimethyl acetal and N,N-diethylformamide dimethyl acetal; N,N-dialkylacetamide dialkyl acetals such as N,N-dimethylacetamide dimethyl acetal and N,N-diethylacetamide dimethyl acetal; and N,N-dialkylpropionamide dialkyl acetals such as N,N-dimethylpropionamide dimethyl acetal and N,N-diethylpropionamide dimethyl acetal. Among them, N,N-dialkylformamide dialkyl acetals are preferable, and N,N-dimethylformamide dimethyl acetals are more preferable.

In a method of producing the conjugated diene polymer, a coupling agent may be added to a solution of the conjugated diene polymer in a hydrocarbon at a time from initiation of the polymerization of monomers until recovery of a polymer described later. Examples of the coupling agent include a compound represented by the following formula (V):
R⁵¹_aML_4-a  (V)
wherein R⁵¹ represents an alkyl group, an alkenyl group, a cycloalkenyl group, or an aryl group; M represents a silicon atom or a tin atom; L represents a halogen atom or a hydrocarbyloxy group; and a represents an integer of 0 to 2.

Examples of the coupling agent represented by the formula (V) include silicon tetrachloride, methyltrichlorosilane, dimethyldichlorosilane, trimethylchlorosilane, tin tetrachloride, methyltrichlorotin, dimethyldichlorotin, trimethylchlorotin, tetramethoxysilane, methyltrimethoxysilane, dimethoxydimethylsilane, methyltriethoxysilane, ethyltrimethoxysilane, dimethoxydiethylsilane, diethoxydimethylsilane, tetraethoxysilane, ethyltriethoxysilane, and diethoxydiethylsilane.

For enhancing the processability of the conjugated diene polymer, the amount of the coupling agent to be added is preferably not less than 0.03 mol and more preferably not less than 0.05 mol, per mol of an alkali metal derived from an alkali metal catalyst. For enhancing the fuel economy, the amount is preferably not more than 0.4 mol and more preferably not more than 0.3 mol.

In the method of producing the conjugated diene polymer, an unreacted active terminal may be treated with alcohol, such as methanol or isopropyl alcohol, before recovery of a polymer described later.

As a method of recovering a conjugated diene polymer from the solution of the conjugated diene polymer in a hydrocarbon, known methods may be employed. Examples of the method include (A) a method of adding a coagulant to the solution of the conjugated diene polymer in a hydrocarbon, and (B) a method of adding steam to the solution of the conjugated diene polymer in a hydrocarbon solvent (steam stripping treatment). The recovered conjugated diene polymer may be dried with a known dryer, such as a band dryer or an extrusion-type dryer.

For achieving a balanced enhancement in processability, fuel economy, rubber strength, abrasion resistance, wet-grip performance, and handling stability, the amount of the structural unit derived from the polymerization initiator represented by the formula (I) in the conjugated diene polymer, when expressed per unit mass of the polymer, is preferably not less than 0.0001 mmol/g polymer, and more preferably not less than 0.001 mmol/g polymer, but is preferably not more than 0.15 mmol/g polymer, and more preferably not more than 0.1 mmol/g polymer.

For achieving a balanced enhancement in processability, fuel economy, rubber strength, abrasion resistance, wet-grip performance, and handling stability, the amount of the structural unit derived from the silicon-containing vinyl compound in the conjugated diene polymer, when expressed per unit mass of the polymer, is preferably not less than 0.01 mmol/g polymer, and more preferably not less than 0.02 mmol/g polymer, but is preferably not more than 0.4 mmol/g polymer, and more preferably not more than 0.2 mmol/g polymer.

For achieving a balanced enhancement in processability, fuel economy, rubber strength, abrasion resistance, wet-grip performance, and handling stability, the conjugated diene polymer preferably contains a structural unit derived from the compound represented by the formula (II). The structural unit derived from the compound represented by the formula (II) in the conjugated diene polymer refers to a structural unit represented by the following formula (IIb):

##STR00017##
wherein m, R²¹, X¹, X², and X³ are the same as those stated in the description of the formula (II).

In the conjugated diene polymer according to the present invention, preferably, at least one of X¹, X² and X³ is replaced by a hydroxyl group, more preferably two or more of X¹, X² and X³ are replaced by hydroxyl groups, and still more preferably two of X¹, X² and X³ are replaced by hydroxyl groups, in the structural unit derived from the compound represented by the formula (II). This enables to enhance the effect of enhancing the processability, fuel economy, rubber strength, abrasion resistance, wet-grip performance, and handling stability. Unlimited examples of a method of replacing at least one of X¹, X², and X³ with a hydroxyl group include steam stripping treatment.

For achieving a balanced enhancement in processability, fuel economy, rubber strength, abrasion resistance, wet-grip performance, and handling stability, the conjugated diene polymer preferably contains a structural unit (aromatic vinyl unit) derived from an aromatic vinyl compound. If the conjugated diene polymer contains an aromatic vinyl unit, the amount of the aromatic vinyl compound in the conjugated diene polymer based on 100% by mass of the combined amount of the structural unit (conjugated diene unit) derived from the conjugated diene compound and the aromatic vinyl unit is preferably not less than 10% by mass (the amount of the conjugated diene unit is not more than 90% by mass), and more preferably not less than 15% by mass (the amount of the conjugated diene unit is not more than 85% by mass). Also, from the viewpoint of the fuel economy, the amount of the aromatic vinyl unit is preferably not more than 50% by mass (the amount of the conjugated diene unit is not less than 50% by mass), and more preferably not more than 45% by mass (the amount of the conjugated diene unit is not less than 55% by mass).

If the conjugated diene polymer contains a structural unit derived from an aromatic vinyl compound, for enhancing the fuel economy, the vinyl bond content (vinyl content) in the conjugated diene polymer is preferably not more than 80 mol %, and more preferably not more than 70 mol %, based on the amount of the conjugated diene unit (regarded as 100 mol %). From the viewpoint of the wet-grip performance, the vinyl bond content is preferably not less than 10 mol %, more preferably not less than 15 mol %, still more preferably not less than 20 mol %, and particularly preferably not less than 40 mol %.

In particular, for enhancing the abrasion resistance, the conjugated diene polymer preferably contains no structural unit derived from an aromatic vinyl compound. In this case, the vinyl bond content (vinyl content) in the conjugated diene polymer is preferably not more than 20 mol %, and more preferably not more than 15 mol %, based on the amount of the conjugated diene unit (regarded as 100 mol %).

The vinyl bond content in the conjugated diene polymer is measured by the method described in examples below.

For enhancing the fuel economy, the molecular weight distribution of the conjugated diene polymer is preferably 1 to 5, and more preferably 1 to 2. The molecular weight distribution is obtained by measuring a number-average molecular weight (Mn) and a weight-average molecular weight (Mw) using gel permeation chromatography (GPC), and dividing Mw by Mn.

The conjugated diene polymer may be used as a rubber component in the rubber composition of the present invention.

The amount of the conjugated diene polymer based on 100% by mass of the rubber component is not more than 90% by mass, preferably not more than 80% by mass, and more preferably not more than 75% by mass. An amount of more than 90% by mass tends to not only decrease the abrasion resistance but also drive up the cost. The amount of the conjugated diene polymer is not less than 1% by mass, preferably not less than 5% by mass, more preferably not less than 10% by mass, still more preferably not less than 25% by mass, and particularly preferably not less than 55% by mass. An amount of less than 1% by mass tends not to easily improve the fuel economy.

The rubber composition of the present invention includes styrene-butadiene rubber (SBR). Examples of the SBR include the conjugated diene polymer synthesized as a modified SBR, and SBRs usually used in the tire industry such as Nipol NS116R (produced by produced by ZEON Corporation).

The amount of SBR based on 100% by mass of the rubber component is not less than 35% by mass, and preferably not less than 45% by mass. If the amount is less than 35% by mass, the handling stability on dry road surfaces or wet-grip performance may not be sufficiently improved. The amount of SBR may be 100% by mass, but is preferably not more than 80% by mass, and more preferably not more than 75% by mass. If the amount exceeds 80% by mass, the fuel economy may decrease.

The amount of SBR refers to the total amount of modified SBRs and unmodified SBRs.

The other rubber component to be used together with the conjugated diene polymer may suitably be a polyisoprene-based rubber. If a polyisoprene-based rubber is added, the rubber strength increases, and the cohesion of the rubber compound during mixing is enhanced so that productivity can be improved.

Examples of the polyisoprene-based rubber include natural rubber (NR), and polyisoprene rubber (IR). The NR is not particularly limited, and examples thereof include those usually used in the tire industry, such as SIR20, RSS#3, TSR20, deproteinized natural rubber (DPNR), highly purified natural rubber (HPNR), and epoxidized natural rubber (ENR). Similarly, IRs usually used in the tire industry may be used.

In the case where the rubber composition of the present invention includes a polyisoprene-based rubber, the amount of the polyisoprene-based rubber based on 100% by mass of the rubber component is preferably not less than 10% by mass, and more preferably not less than 15% by mass. If the amount is less than 10% by mass, the rubber strength may decrease and the cohesion of the rubber compound during mixing may be so poor that productivity can be deteriorated. The amount of the polyisoprene-based rubber is not more than 40% by mass, and preferably not more than 25% by mass. If the amount of the polyisoprene-based rubber exceeds 40% by mass, sufficient wet-grip performance may not be achieved.

Examples of materials that can be used in the rubber component, other than polyisoprene-based rubbers, include polybutadiene rubber (BR), butadiene-isoprene copolymer rubber, and butyl rubber. Ethylene-propylene copolymers, and ethylene-octene copolymers may also be mentioned. Two or more kinds of the rubber materials may be used in combination. From the viewpoint of achieving a balanced improvement in processability, fuel economy, rubber strength, abrasion resistance, wet-grip performance, and handling stability, a rubber component containing not less than 50% by mass of a structural unit derived from a conjugated diene compound is preferably used. Specifically, BR is preferred.

The BR is not particularly limited, and examples thereof include BRs usually used in the tire industry. For example, BRs with a high cis content such as BR1220 (produced by ZEON Corporation), and BR130B and BR150B (produced by Ube Industries, Ltd.); and syndiotactic polybutadiene crystal-containing BRs such as VCR412 and VCR617 (produced by Ube Industries, Ltd.) may be used.

If the rubber composition of the present invention contains BR, the amount of BR based on 100% by mass of the rubber component is preferably not less than 5% by mass, more preferably not less than 10% by mass, and still more preferably not less than 15% by mass. If the amount is less than 5% by mass, the abrasion resistance tends to decrease. The amount of BR is preferably not more than 60% by mass, more preferably not more than 50% by mass, still more preferably not more than 40% by mass, and particularly preferably not more than 30% by mass. If the amount is more than 60% by mass, the wet grip performance tends to decrease.

The rubber composition of the present invention contains silica having a nitrogen adsorption specific surface area (N₂SA) of 40 to 400 m²/g. Unlimited examples of the silica include dry silica (anhydrous silica) and wet silica (hydrous silica). Wet silica is preferable because it has more silanol groups.

The silica has a nitrogen adsorption specific surface area (N₂SA) of not less than 40 m²/g, preferably not less than 50 m²/g, and more preferably not less than 60 m²/g. If the silica has a N₂SA of less than 40 m²/g, the silica tends to have little reinforcement, and thus the abrasion resistance and rubber strength tend to decrease. The silica has a N₂SA of not more than 400 m²/g, preferably not more than 360 m²/g, and more preferably not more than 300 m²/g. Silica having a N₂SA of more than 400 m²/g tends not to disperse easily, and thus the fuel economy and processability tend to deteriorate.

The N₂SA of silica is determined by the BET method in accordance with ASTM D3037-93.

The amount of the silica (total amount if two or more kinds of silica are used) for each 100 parts by mass of the rubber component is not less than 10 parts by mass, preferably not less than 30 parts by mass, and more preferably not less than 45 parts by mass. If the amount is less than 10 parts by mass, the effect producible by blending silica tends not to be sufficiently achieved, and the abrasion resistance and rubber strength tend to decrease. The amount of the silica is not more than 150 parts by mass, and preferably not more than 100 parts by mass. If the amount exceeds 150 parts by mass, the processability tends to deteriorate.

One kind of silica may solely be used, but preferably two or more kinds of silica are used in combination. A combination use of silica (1) having a nitrogen adsorption specific surface area of at least 50 m²/g but less than 120 m²/g, and silica (2) having a nitrogen adsorption specific surface area of not less than 120 m²/g is more preferable. If the silica (1) and the silica (2) are mixed with the conjugated diene polymer, the silica (1) and the silica (2) disperse well so that the effect of improving the properties can be synergistically enhanced. Moreover, if the silica (1) and the silica (2) are used together with a mercapto group-containing silane coupling agent or a specific solid resin, which is described later, the effect of improving the properties can further be enhanced.

The silica (1) and the silica (2) preferably satisfy the inequality: (N₂SA of silica (2))/(N₂SA of silica (1))≧1.4, and more preferably satisfy the inequality: (N₂SA of silica (2))/(N₂SA of silica (1))≧2.0. If the ratio of (N₂SA of silica (2))/(N₂SA of silica (1)) is less than 1.4, the difference in the particle diameter between the silica (1) and the silica (2) is small. Thus, a dispersibility-improving effect producible by blending two kinds of silica tends not to be sufficiently achieved.

The silica (1) has a N₂SA of not less than 50 m²/g, and preferably not less than 70 m²/g. If the silica (1) has a N₂SA of less than 50 m²/g, the silica tends to have an insufficient reinforcement, and the rubber strength, abrasion resistance, and handling stability may deteriorate. The silica (1) has a N₂SA of less than 120 m²/g, and preferably not more than 115 m²/g. If the silica (1) has a N₂SA of not less than 120 m²/g, the effect producible by the combination use of the silica (1) and the silica (2) may not be sufficiently achieved.

The silica (2) has a N₂SA of not less than 120 m²/g, and preferably not less than 150 m²/g. If the silica (2) has a N₂SA of less than 120 m²/g, the effect producible by the combination use of the silica (1) and the silica (2) may not be sufficiently achieved. The silica (2) has a N₂SA of preferably not more than 250 m²/g, and more preferably not more than 220 m²/g. If the silica (2) has a N₂SA of more than 250 m²/g, the fuel economy and processability tend to deteriorate.

The amounts of the silica (1) and the silica (2) preferably satisfy the following inequality:
(Amount of silica (1))×0.06≦(Amount of silica (2))≦(Amount of silica (1))×15.

If the amount of the silica (2) is less than 0.06 times the amount of the silica (1), a sufficient rubber strength tends not to be achieved. If the amount of the silica (2) is more than 15 times the amount of the silica (1), the rolling resistance tends to increase. The amount of the silica (2) is more preferably not less than 0.3 times the amount of the silica (1), and still more preferably not less than 0.5 times the amount of the silica (1). Also, the amount of the silica (2) is more preferably not more than 7 times the amount of the silica (1), and still more preferably not more than 4 times the amount of the silica (1).

The amount of the silica (1) is preferably not less than 5 parts by mass, and more preferably not less than 10 parts by mass for each 100 parts by mass of the rubber component. If the amount of the silica (1) is less than 5 parts by mass, the fuel economy may not be sufficiently improved. Also, the amount of the silica (1) is preferably not more than 90 parts by mass, and more preferably not more than 70 parts by mass. If the amount of the silica (1) is more than 90 parts by mass, good fuel economy is achieved, but the rubber strength and abrasion resistance tend to decrease.

The amount of the silica (2) is preferably not less than 5 parts by mass, and more preferably not less than 10 parts by mass for each 100 parts by mass of the rubber component. If the amount of the silica (2) is less than 5 parts by mass, sufficient handling stability may not be achieved. Also, the amount of the silica (2) is preferably not more than 90 parts by mass, and more preferably not more than 70 parts by mass. If the amount of the silica (2) is more than 90 parts by mass, good handling stability is achieved; however, the processability tends to deteriorate.

The total amount of the silica (1) and the silica (2) is preferably not less than 10 parts by mass, more preferably not less than 30 parts by mass, and still more preferably not less than 45 parts by mass for each 100 parts by mass of the rubber component. If the total amount is less than 10 parts by mass, the effect producible by blending the silica (1) and the silica (2) may not be sufficiently achieved. Thus, the abrasion resistance and rubber strength tend to decrease. The total amount of the silica (1) and the silica (2) is not more than 150 parts by mass, and preferably not more than 100 parts by mass. If the total amount exceeds 150 parts by mass, the processability tends to deteriorate.

The silica may be used together with a silane coupling agent. From a viewpoint that a combination use of the conjugated diene polymer and the silica can synergistically improve the properties, preferable examples of silane coupling agents include mercapto group-containing silane coupling agents. If a mercapto group-containing silane coupling agent is used together with the silica (1) and the silica (2) or a specific solid resin mentioned later, the effect of improving the properties can further be enhanced.

Preferable examples of the mercapto group-containing silane coupling agent include a compound represented by the formula (1) below, and/or a compound containing a linking unit A represented by the formula (2) below and a linking unit B represented by the formula (3) below,

##STR00018##
wherein R¹⁰¹ to R¹⁰³ each represent a branched or unbranched C_1-12 alkyl group, a branched or unbranched C_1-12 alkoxy group, or a group represented by —O— (R¹¹¹—O)_z—R¹¹² where z R¹¹¹s each represent a branched or unbranched C_1-30 divalent hydrocarbon group, and z R¹¹¹s may be the same as or different from one another; R¹¹² represents a branched or unbranched C_1-30 alkyl group, a branched or unbranched C_2-30 alkenyl group, a C_6-30 aryl group, or a C_7-30 aralkyl group; and z represents an integer of 1 to 30, and R¹⁰¹ to R¹⁰³ may be the same as or different from one another; and R¹⁰⁴ represents a branched or unbranched C_1-6 alkylene group;

##STR00019##
wherein R²⁰¹ represents a hydrogen atom, a halogen atom, a branched or unbranched C_1-30 alkyl group, a branched or unbranched C_2-30 alkenyl group, a branched or unbranched C_2-30 alkynyl group, or the alkyl group in which a terminal hydrogen atom is replaced with a hydroxyl group or a carboxyl group; R²⁰² represents a branched or unbranched C_1-30 alkylene group, a branched or unbranched C_2-30 alkenylene group, or a branched or unbranched C_2-30 alkynylene group; and R²⁰¹ and R²⁰² may be joined together to form a cyclic structure.

The following describes the compound represented by the formula (I).

The use of the compound represented by the formula (1) allows the silica to disperse well, and thus the effects of the present invention are well achieved. In particular, the use of the compound represented by the formula (1) can greatly improve the wet grip performance and fuel economy.

R¹⁰¹ to R¹⁰³ each are a branched or unbranched C_1-12 alkyl group, a branched or unbranched C_1-12 alkoxy group, or a group represented by —O—(R¹¹¹—O)_z—R¹¹². In view of achieving the effects of the present invention well, preferably at least one of R¹⁰¹ to R¹⁰³ is a group represented by —O—(R¹¹¹—O)_z—R¹¹², and more preferably two of R¹⁰¹ to R¹⁰³ are groups represented by —O—(R¹¹¹—O)_z—R¹¹² and the other is a branched of unbranched C_1-12 alkoxy group.

Examples of the branched or unbranched C_1-12 (preferably C_1-5) alkyl group for R¹⁰¹ to R¹⁰³ include a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, an iso-butyl group, a sec-butyl group, a tert-butyl group, a pentyl group, a hexyl group, a heptyl group, a 2-ethylhexyl group, an octyl group, and a nonyl group.

Examples of the branched or unbranched C_1-12 (preferably C_1-5) alkoxy group for R¹⁰¹ to R¹⁰³ include a methoxy group, an ethoxy group, an n-propoxy group, an isopropoxy group, an n-butoxy group, an iso-butoxy group, a sec-butoxy group, a tert-butoxy group, a pentyloxy group, a hexyloxy group, a heptyloxy group, a 2-ethylhexyloxy group, an octyloxy group, and a nonyloxy group.

R¹¹¹ in the group represented by —O—(R¹¹¹—O)_z—R¹¹² for R¹⁰¹ to R¹⁰³ represents a branched or unbranched C_1-30 (preferably C_1-15, more preferably C_1-3) divalent hydrocarbon group.

Examples of the hydrocarbon group include branched or unbranched C_1-30 alkylene groups, branched or unbranched C_2-30 alkenylene groups, branched or unbranched C_2-30 alkynylene groups, and branched or unbranched C_6-30 arylene groups. Branched or unbranched C_1-30 alkylene groups are preferred among the examples.

Examples of the branched or unbranched C_1-30 (preferably C_1-15, more preferably C_1-3) alkylene group for R¹¹¹ include a methylene group, an ethylene group, a propylene group, a butylene group, a pentylene group, a hexylene group, a heptylene group, an octylene group, a nonylene group, a decylene group, an undecylene group, a dodecylene group, a tridecylene group, a tetradecylene group, a pentadecylene group, a hexadecylene group, a heptadecylene group, and an octadecylene group.

Examples of the branched or unbranched C_2-30 (preferably C_2-15, more preferably C_2-3) alkenylene group for R¹¹¹ include a vinylene group, a 1-propenylene group, a 2-propenylene group, a 1-butenylene group, a 2-butenylene group, a 1-pentenylene group, a 2-pentenylene group, a 1-hexenylene group, a 2-hexenylene group, and a 1-octenylene group.

Examples of the branched or unbranched C_2-30 (preferably C_2-15, more preferably C_2-3) alkynylene group for R¹¹¹ include an ethynylene group, a propynylene group, a butynylene group, a pentynylene group, a hexynylene group, a heptynylene group, an octynylene group, a nonynylene group, a decynylene group, an undecynylene group, and a dodecynylene group.

Examples of the C_6-30 (preferably C_6-15) arylene group for R¹¹¹ include a phenylene group, a tolylene group, a xylylene group, and a naphthylene group.

Here, z represents an integer of 1 to 30 (preferably 2 to 20, more preferably 3 to 7, and still more preferably 5 or 6).

R¹¹² represents a branched or unbranched C_1-30 alkyl group, a branched or unbranched C_2-30 alkenyl group, a C_6-30 aryl group, or a C_7-30 aralkyl group. R¹¹² is especially preferably a branched or unbranched C_1-30 alkyl group.

Examples of the branched or unbranched C_1-30 (preferably C_3-25, more preferably C_10-15) alkyl group for R¹¹² include a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, an iso-butyl group, a sec-butyl group, a tert-butyl group, a pentyl group, a hexyl group, a heptyl group, a 2-ethylhexyl group, an octyl group, a nonyl group, a decyl group, an undecyl group, a dodecyl group, a tridecyl group, a tetradecyl group, a pentadecyl group, and an octadecyl group.

Examples of the branched or unbranched C_2-30 (preferably C_3-25, more preferably C_10-15) alkenyl group for R¹¹² include a vinyl group, a 1-propenyl group, a 2-propenyl group, a 1-butenyl group, a 2-butenyl group, a 1-pentenyl group, a 2-pentenyl group, a 1-hexenyl group, a 2-hexenyl group, a 1-octenyl group, a decenyl group, an undecenyl group, a dodecenyl group, a tridecenyl group, a tetradecenyl group, a pentadecenyl group, and an octadecenyl group.

Examples of the C_6-30 (preferably C_10-20) aryl group for R¹¹² include a phenyl group, a tolyl group, a xylyl group, a naphthyl group, and a biphenyl group.

Examples of the C_7-30 (preferably C_10-20) aralkyl group for R¹¹² include a benzyl group and a phenethyl group.

Specific examples of the group represented by —O—(R¹¹¹—O)_z—R¹¹² include groups represented by —O—(C₂H₄—O)₅—C₁₁H₂₃, —O—(C₂H₄—O)₅—C₁₂R₂₅, —O—(C₂H₄—O)₅—C₁₃H₂₇, —O—(C₂H₄—O)₅—C₁₄H₂₉, —O—(C₂H₄—O)₅—C₁₅H₃₁, —O—(C₂H₄—O)₃—C₁₃H₂₇, —O—(C₂H₄—O)₄—C₁₃H₂₇, —O—(C₂H₄—O)₆—C₁₃H₂₇ and —O—(C₂H₄—O)₇—C₁₃H₂₇. Among the examples, groups represented by —O—(C₂H₄—O)₅—C₁₁H₂₃, —O—(C₂H₄—O)₅—C₁₃H₂₇, —O—(C₂H₄—O)₅—C₁₅H₃₁, and —O—(C₂H₄—O)₆—C₁₃H₂₇ are preferable.

Examples of the branched or unbranched C_1-6 (preferably C_1-5) alkylene group for R¹⁰⁴ include groups as mentioned for the branched or unbranched C_1-30 alkylene groups for R¹¹¹.

Examples of the compound represented by the formula (1) include 3-mercaptopropyltrimethoxysilane, 3-mercaptopropyltriethoxysilane, 2-mercaptoethyl-trimethoxysilane, 2-mercaptoethyltriethoxysilane, and a compound represented by the following formula (Si363 produced by Evonik Degussa). Use of the compound represented by the following formula is preferred. Any of these compounds may be used alone or two or more of these may be used in combination.

##STR00020##

The following describes the compound containing a linking unit A represented by the formula (2) and a linking unit B represented by the formula (3).

In the case where the compound containing a linking unit A represented by the formula (2) and a linking unit B represented by the formula (3) is used, the increase in viscosity during the processing is suppressed as compared to the case where polysulfide silane such as bis-(3-triethoxysilylpropyl)tetrasulfide is used. This is presumably because, since the sulfide moiety of the linking unit A is a C—S—C bond, the compound is thermally more stable than tetrasulfide or disulfide, and thus the Mooney viscosity is less likely to increase.

Moreover, the decrease in the scorch time is suppressed compared to the case where mercapto silane such as 3-mercaptopropyltrimethoxysilane is used. This is presumably because, though the linking unit B has a mercapto silane structure, the —C₇H₁₅ moiety of the linking unit A covers a —SH group of the linking unit B, as a result of which the SH group is less likely to react with polymers. Thus, scorch is less likely to occur.

From the viewpoint of enhancing the effects of suppressing the viscosity increase during the processing and of suppressing the decrease in the scorch time as mentioned above, the linking unit A content in the silane coupling agent having the foregoing structure is preferably not less than 30 mol %, and more preferably not less than 50 mol %, but is preferably not more than 99 mol %, and more preferably not more than 90 mol %. The linking unit B content is preferably not less than 1 mol %, more preferably not less than 5 mol %, and still more preferably not less than 10 mol %, but is preferably not more than 70 mol %, more preferably not more than 65 mol %, and still more preferably not more than 55 mol %. The combined amount of the linking unit A and the linking unit B is preferably not less than 95 mol %, more preferably not less than 98 mol %, and particularly preferably 100 mol %.

The amount of the linking unit A or B is the amount including the linking unit A or B that is present at the terminal of the silane coupling agent, if any. In the case where the linking unit A or B is present at the terminal of the silane coupling agent, its form is not particularly limited as long as it forms a unit corresponding to the formula (2) representing the linking unit A or the formula (3) representing the linking unit B.

Examples of the halogen atom for R²⁰¹ include chlorine, bromine, and fluorine.

Examples of the branched or unbranched C_1-30 alkyl group for R²⁰¹ include a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, an iso-butyl group, a sec-butyl group, a tert-butyl group, a pentyl group, a hexyl group, a heptyl group, a 2-ethylhexyl group, an octyl group, a nonyl group, and a decyl group. The alkyl group preferably has 1 to 12 carbon atom(s).

Examples of the branched or unbranched O_2-30 alkenyl group for R²⁰¹ include a vinyl group, a 1-propenyl group, a 2-propenyl group, a 1-butenyl group, a 2-butenyl group, a 1-pentenyl group, a 2-pentenyl group, a 1-hexenyl group, a 2-hexenyl group, and a 1-octenyl group. The alkenyl group preferably has 2 to 12 carbon atoms.

Examples of the branched or unbranched C_2-30 alkynyl group for R²⁰¹ include an ethynyl group, a propynyl group, a butynyl group, a pentynyl group, a hexynyl group, a heptynyl group, an octynyl group, a nonynyl group, a decynyl group, an undecynyl group, and a dodecynyl group. The alkynyl group preferably has 2 to 12 carbon atoms.

Examples of the branched or unbranched C_1-30 alkylene group for R²⁰² include an ethylene group, a propylene group, a butylene group, a pentylene group, a hexylene group, a heptylene group, an octylene group, a nonylene group, a decylene group, an undecylene group, a dodecylene group, a tridecylene group, a tetradecylene group, a pentadecylene group, a hexadecylene group, a heptadecylene group, and an octadecylene group. The alkylene group preferably has 1 to 12 carbon atom(s).

Examples of the branched or unbranched C_2-30 alkenylene group for R²⁰² include a vinylene group, a 1-propenylene group, a 2-propenylene group, a 1-butenylene group, a 2-butenylene group, a 1-pentenylene group, a 2-pentenylene group, a 1-hexenylene group, a 2-hexenylene group, and a 1-octenylene group. The alkenylene group preferably has 2 to 12 carbon atoms.

Examples of the branched or unbranched C_2-30 alkynylene group for R²⁰² include an ethynylene group, a propynylene group, a butynylene group, a pentynylene group, a hexynylene group, a heptynylene group, an octynylene group, a nonynylene group, a decynylene group, an undecynylene group, and a dodecynylene group. The alkynylene group preferably has 2 to 12 carbon atoms.

In the compound containing the linking unit A represented by the formula (2) and the linking unit B represented by the formula (3), the total number of repetitions (x+y) of the number of repetitions (x) of the linking unit A and the number of repetitions (y) of the linking unit B is preferably in the range of 3 to 300. If the total number of repetitions is in the range mentioned above, the —C₇H₁₅ moiety of the linking unit A covers the mercaptosilane of the linking unit B, which enables not only to suppress the decrease in the scorch time but also to surely achieve good reactivity to silica and the rubber component.

Examples of the compound containing the linking unit A represented by the formula (2) and the linking unit B represented by the formula (3) include NXT-Z30, NXT-Z45, and NXT-Z60 (produced by Momentive Performance Materials). Any of these may be used alone, or two or more of these may be used in combination.

The amount of the mercapto group-containing silane coupling agent is preferably not less than 0.5 parts by mass, and more preferably not less than 3 parts by mass for each 100 parts by mass of the silica. If the amount is less than 0.5 parts by mass, the resulting unvulcanized rubber composition tends to have high viscosity. Thus, sufficient processability may not be surely achieved. Also, the amount of the mercapto group-containing silane coupling agent is preferably not more than 20 parts by mass, and more preferably not more than 10 parts by mass. If the amount exceeds 20 parts by mass, the rubber strength and abrasion resistance tend to deteriorate.

The rubber composition of the present invention preferably includes other silane coupling agents as well as the mercapto group-containing silane coupling agent. This enables to enhance the effect of improving the properties. Examples of other silane coupling agents include bis(3-triethoxysilylpropyl)tetrasulfide, bis(3-triethoxysilylpropyl)trisulfide, bis(3-triethoxysilylpropyl)disulfide, bis(2-triethoxysilylethyl)tetrasulfide, 3-trimethoxysilylpropyl-N,N-dimethylthiocarbamoyl tetrasulfide, bis(3-trimethoxysilylpropyl)tetrasulfide, bis(2-trimethoxysilylethyl)tetrasulfide, 3-triethoxysilylpropyl-N,N-dimethylthiocarbamoyl tetrasulfide, 2-triethoxysilylethyl-N,N-dimethylthiocarbamoyl tetrasulfide, 3-trimethoxysilylpropylbenzothiazole tetrasulfide, 3-triethoxysilylpropylbenzothiazolyl tetrasulfide, 3-triethoxysilylpropylmethacrylate monosulfide, 3-trimethoxysilylpropylmethacrylate monosulfide, bis(3-diethoxymethylsilylpropyl)tetrasulfide, 3-mercaptopropyldimethoxymethylsilane, dimethoxymethylsilylpropyl-N,N-dimethylthiocarbamoyl tetrasulfide, and dimethoxymethylsilylpropylbenzothiazole tetrasulfide. Preferred among these is bis(3-triethoxysilylpropyl)tetrasulfide.

The amount of the other silane coupling agent is preferably not less than 0.5 parts by mass, and more preferably not less than 3 parts by mass for each 100 parts by mass of the silica. If the amount is less than 0.5 parts by mass, the resulting unvulcanized rubber composition has high viscosity. Thus, sufficient processability may not be surely achieved. Also, the amount of the other silane coupling agent is preferably not more than 20 parts by mass, and more preferably not more than 10 parts by mass. If the amount exceeds 20 parts by mass, the rubber strength and abrasion resistance tend to deteriorate.

The total amount of the silane coupling agents is preferably not less than 0.5 parts by mass, and more preferably not less than 3 parts by mass for each 100 parts by mass of the silica. If the amount is less than 0.5 parts by mass, the resulting unvulcanized rubber composition has high viscosity. Thus, sufficient processability may not be surely achieved. Also, the total amount of the silane coupling agents is preferably not more than 20 parts by mass, and more preferably not more than 10 parts by mass. If the total amount exceeds 20 parts by mass, the rubber strength and abrasion resistance tend to deteriorate.

The rubber composition of the present invention preferably includes a solid resin having a glass transition temperature of 60 to 120° C. If the solid resin is used together with the conjugated diene polymer, the effect of improving the properties can be synergistically enhanced. Moreover, if the solid resin is used together with the mercapto group-containing silane coupling agent, or the silica (1) and the silica (2), the effect of improving the properties can further be enhanced.

The solid resin has a glass transition temperature (Tg) of not lower than 60° C., and preferably not lower than 75° C. If the solid resin has a glass transition temperature of lower than 60° C., the effect of improving the wet-grip performance may not be sufficiently achieved. The solid resin has a Tg of not higher than 120° C., and preferably not higher than 100° C. If the solid resin has a Tg of higher than 120° C., the loss elastic modulus at high temperature ranges increases greatly so that the fuel economy tends to deteriorate.

The Tg of the solid resin is a value (midpoint glass transition temperature) measured at a rate of temperature rise of 10° C./min. with a differential scanning calorimeter Q200 (produced by TA Instruments Japan Inc.) in accordance with JIS-K7121.

Any solid resin may be used as the solid resin as long as it has a Tg mentioned above. Examples of the solid resin include an aromatic resin, such as an aromatic vinyl polymer prepared by polymerizing α-methyl styrene and/or styrene, a coumarone-indene resin, or an indene resin; a terpene resin; and a rosin resin. The derivatives of those resins may also be used. An aromatic resin is preferable, and an aromatic vinyl polymer prepared by polymerizing α-methyl styrene and/or styrene and a coumarone-indene resin are more preferable, as the use of such solid rubber enables to provide an unvulcanized rubber composition with good adhesion property and to achieve good fuel economy.

Styrene and/or α-methyl styrene is used as an aromatic vinyl monomer (unit) of the aromatic vinyl polymer prepared by polymerizing α-methyl styrene and/or styrene (resin obtained by polymerizing α-methyl styrene and/or styrene). The aromatic vinyl polymer may be a homopolymer of one monomer, or a copolymer of both monomers. Preferably, the aromatic vinyl polymer is a homopolymer of α-methyl styrene, or a copolymer of α-methyl styrene and styrene as use of such a homopolymer or copolymer is cost efficient, and enables to achieve good processability and excellent wet-grip performance.

The aromatic vinyl polymer has a weight-average molecular weight (Mw) of preferably not less than 500, and more preferably not less than 800. If the Mw is less than 500, the effect of improving the wet-grip performance tends not to be easily achieved sufficiently. The aromatic vinyl polymer has a weight-average molecular weight of preferably not more than 3000, and more preferably not more than 2000. If the Mw is more than 3000, the dispersibility of the filler decreases so that the fuel economy tends to deteriorate.

Herein, the weight-average molecular weight can be measured using gel permeation chromatography (GPC) (GPC-8000 series produced by Tosoh Corporation, detector: differential refractometer) and expressed as a polystyrene-equivalent value.

The coumarone-indene resin and the indene resin are a coal or petroleum resin containing coumarone having eight carbon atoms and indene having nine carbon atoms as principal monomers, and a coal or petroleum resin containing indene as a principal monomer, respectively. Specific examples thereof include vinyltoluene-α-methylstyrene-indene resin, vinyltoluene-indene resin, α-methylstyrene-indene resin, and α-methylstyrene-vinyltoluene-indene copolymer resin.

The terpene resin is a resin that is derived from, as a principal monomer, a terpene compound having a terpene backbone such as a monoterpene, a sesquiterpene or a diterpene. Examples thereof include α-pinene resin, β-pinene resin, limonene resin, dipentene resin, β-pinene/limonene resins, aromatic modified terpene resin, terpene phenolic resin, and hydrogenated terpene resin. Examples of the rosin resin include natural rosin resin (polymerized rosin) such as gum rosin, wood rosin and tall oil rosin, hydrogenated rosin resins, maleic acid-modified rosin resin, rosin-modified phenolic resin, rosin glycerol esters, and disproportionated rosin resin. Natural rosin resins can be produced by processing pine resin, and each mainly contains a resin acid such as abietic acid or pimaric acid.

The amount of the solid resin is preferably not less than 1 part by mass, more preferably not less than 3 parts by mass, and still more preferably not less than 5 parts by mass for each 100 parts by mass of the rubber component. If the amount is less than 1 part by mass, the effect of improving the wet-grip performance tends not to be sufficiently achieved. The amount of the solid resin is preferably not more than 30 parts by mass, and more preferably not more than 15 parts by mass. If the amount is more than 30 parts by mass, the elastic modulus of the rubber composition at low temperature ranges increases greatly. Thus, the grip performance on snowy roads and the wet-grip performance in cold regions tend to deteriorate.

The rubber composition of the present invention preferably includes at least one liquid resin having a glass transition temperature of −40 to 20° C. selected from the group consisting of aromatic petroleum resins, terpene resins, and rosin resins, and/or a plasticizer having a glass transition temperature of −40 to 20° C. The rubber composition more preferably includes the solid resin as well as the liquid resin and/or the plasticizer. This enables not only to improve the grip performance in wide temperature ranges but also to improve the rubber strength while maintaining the fuel economy.

The liquid resin and the plasticizer each have a Tg of not lower than −40° C., and preferably not lower than −20° C. A Tg of lower than −40° C. excessively increases the action of plasticizing rubber so that the abrasion resistance tends to deteriorate. The liquid resin and the plasticizer each have a Tg of not higher than 20° C., and preferably not higher than 10° C. A Tg of higher than 20° C. leads to a large loss elastic modulus so that the fuel economy tends to deteriorate.

The Tg of the liquid resin and that of the plasticizer are values (midpoint glass transition temperatures) measured at a rate of temperature rise of 10° C./min. with a differential scanning calorimeter Q200 (produced by TA Instruments Japan Inc.) in accordance with JIS-K7121.

The liquid resin to be used is at least one selected form the group consisting of aromatic petroleum resins, terpene resins, and rosin resins. An aromatic petroleum resin is preferable as it has a higher effect of improving the rubber strength.

The aromatic petroleum resin applicable as the liquid resin is a resin obtained by polymerizing an aromatic fraction having 9 carbon atoms (C9) containing, as a principal monomer, vinyl toluene or indene which is usually produced by thermal decomposition of naphtha. Examples thereof include low molecular weight forms listed for the solid resin, such as an aromatic vinyl polymer prepared by polymerizing α-methyl styrene and/or styrene, a coumarone resin, or a coumarone-indene resin. Preferred among these are a homopolymer of α-methyl styrene, a copolymer of α-methyl styrene and styrene, a coumarone resin, and a coumarone-indene resin, and more preferred is a coumarone-indene resin, as these resins have a higher effect of improving the rubber strength, abrasion resistance, and wet-grip performance.

Examples of commercially available products of such resins include NOVARES C10 (produced by Rutgers chemicals AG), and Picco A-10 (produced by Eastoman Chemical Company).

Low molecular weight forms of the terpene resins and the rosin resins listed for the solid resin may be used as the liquid resin. Examples of commercially available products of the terpene resin that can be used as the liquid resin include YS resin PX300, YS resin PX300N, Dimerone, and YS Polyster T30 (produced by Yasuhara Chemical Co., Ltd.). Examples of commercially available products of the rosin resin that can be used as the liquid resin include HARIESTER SK-501NS (produced by Harima Chemicals, Inc.).

Any plasticizer may be used as the plasticizer as long as it has a Tg mentioned above. Examples of the plasticizer include a diene polymer having a weight average molecular weight (Mw) of 3,000 to 150,000. In the case of using a diene polymer as the plasticizer, a diene polymer having an epoxidation degree of not more than 25 mol % is preferably used.

The combined amount of the liquid resin and the plasticizer is preferably not less than 1 part by mass, and more preferably not less than 5 parts by mass for each 100 parts by mass of the rubber component. If the combined amount is less than 1 part by mass, the rubber strength and the grip performance in wide temperature ranges may not be sufficiently improved. The combined amount is preferably not more than 30 parts by mass, more preferably not more than 20 parts by mass, and still more preferably not more than 10 parts by mass. If the combined amount is more than 30 parts by mass, the rigidity of the rubber composition tends to be greatly impaired, and the handling stability tend to decrease.

The combined amount of the solid resin, the liquid resin and the plasticizer for each 100 parts by mass of the rubber component is preferably not less than 2 parts by mass, and more preferably not less than 6 parts by mass, but is preferably not more than 60 parts by mass, more preferably not more than 30 parts by mass, and still more preferably not more than 20 parts by mass. If the combined amount is within the range mentioned above, balanced improvements in processability, fuel economy, rubber strength, abrasion resistance, wet-grip performance, and handling stability can be achieved at high levels.

Known additives may be used, and examples thereof include vulcanization agents such as sulfur; vulcanization accelerators such as a thiazole-based vulcanization accelerator, a thiuram-based vulcanization accelerator, a sulfenamide-based vulcanization accelerator, and a guanidine-based vulcanization accelerator; vulcanization activating agents such as stearic acid and zinc oxide; organic peroxides; fillers such as carbon black, calcium carbonate, talc, alumina, clay, aluminum hydroxide, and mica; processing aids such as extender oils and lubricants; and antioxidants.

Examples of the carbon black include furnace black (furnace carbon black) such as SAF, ISAF, HAF, MAF, FEF, SRF, GPF, APF, FF, CF, SCF or ECF; acetylene black (acetylene carbon black); thermal black (thermal carbon black) such as FT or MT; channel black (channel carbon black) such as EPC, MPC or CC; and graphite. Any of these may be used alone or two or more of these may be used in combination.

The amount of carbon black is preferably not less than 1 part by mass, and more preferably not less than 3 parts by mass for each 100 parts by mass of the rubber component. If the amount is less than 1 part by mass, sufficient reinforcement may not be achieved. Also, the amount of carbon black is preferably not more than 60 parts by mass, more preferably not more than 30 parts by mass, and still more preferably not more than 15 parts by mass. If the amount is more than 60 parts by mass, the fuel economy tends to deteriorate.

The nitrogen adsorption specific surface area (N₂SA) of carbon black is usually 5 to 200 m²/g, and preferably the lower limit and the upper limit thereof are 50 m²/g and 150 m²/g, respectively. The dibutyl phthalate (DBP) absorption of carbon black is usually 5 to 300 mL/100 g, and preferably the lower limit and the upper limit thereof are 80 mL/100 g and 180 mL/100 g, respectively. If the N₂SA or DBP absorption of carbon black is lower than the lower limit of the range mentioned above, the reinforcement is small, and the abrasion resistance tends to decrease. If the N₂SA or DBP absorption of carbon black is larger than the upper limit of the range mentioned above, the carbon black does not disperse well, and the hysteresis loss increases. Thus, the fuel economy tends to deteriorate. The nitrogen adsorption specific surface area is measured in accordance with ASTM D4820-93. The DBP absorption is measured in accordance with ASTM D2414-93. Examples of commercially available carbon black include SEAST 6, SEAST 7HM, and SEAST KH (trade name, produced by Tokai Carbon Co., Ltd.), and CK 3 and Special Black 4A (trade name, produced by Evonik Degussa).

Examples of the extender oil include aromatic mineral oils (viscosity gravity constant (V.G.C. value) 0.900 to 1.049), naphthenic mineral oils (V.G.C. value 0.850 to 0.899), and paraffinic mineral oils (V.G.C. value 0.790 to 0.849). The polycyclic aromatic content in the extender oil is preferably less than 3% by mass, and more preferably less than 1% by mass. The polycyclic aromatic content is measured according to the British Institute of Petroleum 346/92 Method. The aromatic compound (CA) content in the extender oil is preferably not less than 20% by mass or more. Two or more kinds of these extender oils may be used in combination.

Examples of the vulcanization accelerator include thiazole-based vulcanization accelerators such as 2-mercaptobenzothiazole, dibenzothiazyl disulfide, and N-cyclohexyl-2-benzothiazylsulfenamide; thiuram-based vulcanization accelerators such as tetramethylthiuram monosulfide and tetramethylthiuram disulfide; sulfenamide-based vulcanization accelerators such as N-cyclohexyl-2-benzothiazolesulfenamide, N-t-butyl-2-benzothiazolesulfenamide, N-oxyethylene-2-benzothiazolesulfenamide, N-oxyethylene-2-benzothiazolesulfenamide, and N,N′-diisopropyl-2-benzothiazolesulfenamide; and guanidine-based vulcanization accelerators such as diphenylguanidine, diorthotolylguanidine, and orthotolylbiguanidine. The amount thereof to be used is preferably 0.1 to 5 parts by mass, and more preferably 0.2 to 3 parts by mass for each 100 parts by mass of the rubber component.

Known methods may be employed for producing a rubber composition by adding other rubber materials and additives to the conjugated diene polymer. Examples of the method include a method of kneading components with a known mixer such as a roll mill or a Banbury mixer.

With regard to the kneading conditions for the case where additives other than the vulcanization agent and the vulcanization accelerator are mixed, the kneading temperature is usually 50 to 200° C., and preferably 80 to 190° C., and the kneading time is usually 30 seconds to 30 minutes, and preferably 1 minute to 30 minutes.

In the case where the vulcanization agent and the vulcanization accelerator are mixed, the kneading temperature is usually not higher than 100° C., and preferably room temperature to 80° C. The composition containing a vulcanization agent and a vulcanization accelerator is usually used after it is vulcanized by press vulcanization or the like. The vulcanization temperature is usually 120 to 200° C., and preferably 140 to 180° C.

The rubber composition of the present invention has a tan δ peak temperature of preferably not lower than −16° C. The rubber composition having a tan δ peak temperature of lower than −16° C. may fail to exert sufficient wet-grip performance required for summer tires. The rubber composition of the present invention has a tan δ peak temperature of preferably not higher than −5° C., and more preferably not higher than −8° C. The rubber composition having a tan δ peak temperature of higher than −5° C. has high temperature dependence, and thus tends not to exert sufficient wet-grip performance in wide temperature ranges.

The tan δ peak temperature is measured by the method described in examples below.

The rubber composition of the present invention is excellent in the balance among processability, fuel economy, rubber strength, abrasion resistance, wet-grip performance, and handling stability, and has effects of significantly improving these properties.

The rubber composition of the present invention may be used in a component of a tire, suitably in a tread (particularly a tread of summer tires).

The pneumatic tire of the present invention is formed from the rubber composition by a usual method. Namely, before vulcanization, the rubber composition optionally containing various additives is extruded and processed into the shape of a tire component (e.g., tread), and then molded in a normal manner on a tire building machine and assembled with other tire components to provide an unvulcanized tire. Then, the unvulcanized tire is heated and pressed in a vulcanizer into a pneumatic tire. Thus, the pneumatic tire of the present invention can be produced.

The pneumatic tire of the present invention can be suitably used as summer tires (particularly, summer tires for passenger vehicles).

EXAMPLES

The present invention is more specifically described based on examples. However, the present invention is not limited thereto.

The following is a list of chemical agents used in the synthesis or polymerization. The chemical agents were purified as needed by usual methods.

THF: anhydrous tetrahydrofuran, produced by Kanto Chemical Co., Inc.

Sodium hydride: produced by Kanto Chemical Co., Inc.

Diethylamine: produced by Kanto Chemical Co., Inc.

Methylvinyldichlorosilane: produced by Shin-Etsu Chemical Co., Ltd.

Anhydrous hexane: produced by Kanto Chemical Co., Inc.

Styrene: produced by Kanto Chemical Co., Inc.

Butadiene: 1,3-butadiene, produced by Tokyo Chemical Industry Co., Ltd.

TMEDA: tetramethylethylenediamine, produced by Kanto Chemical Co., Inc.

n-Butyllithium solution: 1.6 M n-butyllithium in hexane, produced by Kanto Chemical Co., Inc.

Initiator (1): AI-200CE2 (compound prepared by bonding 3-(N,N-dimethylamino)-1-propyllithium and two isoprene-derived structural units, represented by the following formula) (0.9 M), produced by FMC

##STR00021##
Piperidine: produced by Tokyo Chemical Industry Co., Ltd.
Diamylamine: produced by Tokyo Chemical Industry Co., Ltd.
2,6-Di-tert-butyl-p-cresol: Nocrac 200, produced by Ouchi Shinko Chemical Industrial Co., Ltd.
Bis(dimethylamino)methylvinylsilane: produced by Shin-Etsu Chemical Co., Ltd.
N,N-dimethylaminopropylacrylamide: produced by Tokyo Chemical Industry Co., Ltd.
3-Diethylaminopropyltriethoxysilane: produced by Azmax Co., Ltd.
1,3-Dimethyl-2-imidazolidinone: produced by Tokyo Chemical Industry Co., Ltd.
N-phenyl-2-pyrrolidone: produced by Tokyo Chemical Industry Co., Ltd.
N-methyl-ε-caprolactam: produced by Tokyo Chemical Industry Co., Ltd.
Tris[3-(trimethoxysilyl)propyl]isocyanurate: produced by Shin-Etsu Chemical Co., Ltd.
N,N-dimethylformamide dimethyl acetal: produced by Tokyo Chemical Industry Co., Ltd.
1,3-Diisopropenylbenzene: produced by Tokyo Chemical Industry Co., Ltd.
sec-Butyllithium solution: produced by Kanto Chemical Co., Inc. (1.0 mol/L)
Cyclohexane: produced by Kanto Chemical Co., Inc.
<Production of Modifier (1) (Main Chain Modifier)>

In a nitrogen atmosphere, 15.8 g of bis(dimethylamino)methylvinylsilane was charged into a 100-mL volumetric flask, and also anhydrous hexane was added to increase the total amount to 100 mL. In this manner, a modifier (1) was produced.

<Production of Modifier (2) (Terminal Modifier)>

In a nitrogen atmosphere, 15.6 g of N,N-dimethylaminopropylacrylamide was charged into a 100-mL volumetric flask, and also anhydrous hexane was added to increase the total amount to 100 mL. In this manner, a modifier (2) was produced.

<Production of Modifier (3) (Main Chain Modifier)>

THF (1000 mL) and sodium hydride (13 g) were charged into a sufficiently nitrogen-purged 2-L three-necked flask, and diethylamine (36.5 g) was slowly added dropwise thereto on an ice water bath while stirring. After stirring for 30 minutes, methylvinyldichlorosilane (36 g) was added dropwise over 30 minutes, followed by stirring for 2 hours. The resulting solution was concentrated, filtered, and purified by distillation under reduced pressure to give bis(diethylamino)methylvinylsilane. The bis(diethylamino)methylvinylsilane (21.4 g) was charged into a 100-mL volumetric flask in a nitrogen atmosphere, and also anhydrous hexane was added to increase the total amount to 100 mL. In this manner, a modifier (3) was produced.

<Production of Initiator (2)>

Anhydrous hexane (127.6 mL) and piperidine (8.5 g) were charged into a sufficiently nitrogen-purged 200-mL recovery flask, and cooled to 0° C. Then, an n-butyllithium solution (62.5 mL) was slowly added over 1 hour to give an initiator (2).

<Production of Initiator (3)>

Anhydrous hexane (117 mL) and diamylamine (15.7 g) were charged into a sufficiently nitrogen-purged 200-mL recovery flask, and cooled to 0° C. Then, an n-butyllithium solution (62.5 mL) was slowly added over 1 hour to give an initiator (3).

<Production of Modifier (4) (Terminal Modifier)>

In a nitrogen atmosphere, 3-diethylaminopropyltriethoxysilane (27.7 g) was charged into a 100-mL volumetric flask, and also anhydrous hexane was added to increase the total amount to 100 mL. In this manner, a modifier (4) was produced.

<Production of Initiator (4) (Bifunctional Initiator)>

Cyclohexane (550 mL), TMEDA (27 mL), and a sec-butyllithium solution (200 mL) were charged into a sufficiently dried and nitrogen-purged 1-L recovery flask. While the mixture was stirred at 45° C., 1,3-diisopropenylbenzene (17 mL) was slowly added thereto over 30 minutes. The resulting mixed solution was stirred for another 1 hour, and then cooled to room temperature to give an initiator (4).

<Production of Modifier (5) (Terminal Modifier)>

In a nitrogen atmosphere, 1,3-dimethyl-2-imidazolidinone (11.4 g) was charged into a 100-mL volumetric flask, and also anhydrous hexane was added to increase the total amount to 100 mL. In this manner, a modifier (5) was produced.

<Production of Modifier (6) (Terminal Modifier)>

In a nitrogen atmosphere, N-phenyl-2-pyrrolidone (16.1 g) was charged into a 100-mL volumetric flask, and also anhydrous hexane was added to increase the total amount to 100 mL. In this manner, a modifier (6) was produced.

<Production of Modifier (7) (Terminal Modifier)>

In a nitrogen atmosphere, N-methyl-ε-caprolactam (12.7 g) was charged into a 100-mL volumetric flask, and also anhydrous hexane was added to increase the total amount to 100 mL. In this manner, a modifier (7) was produced.

<Production of Modifier (8) (Terminal Modifier)>

In a nitrogen atmosphere, tris[3-(trimethoxysilyl)propyl]isocyanurate (30.7 g) was charged into a 100-mL volumetric flask, and also anhydrous hexane was added to increase the total amount to 200 mL. In this manner, a modifier (8) was produced.

<Production of Modifier (9) (Terminal Modifier)>

In a nitrogen atmosphere, N,N-dimethylformamide dimethyl acetal (11.9 g) was charged into a 100-mL volumetric flask, and also anhydrous hexane was added to increase the total amount to 200 mL. In this manner, a modifier (9) was produced.

<Copolymer Analysis>

Copolymers (conjugated diene polymers) obtained as mentioned later were analyzed by the following methods.

<Measurement of Weight-Average Molecular Weight (Mw) and Number-Average Molecular Weight (Mn)>

The weight-average molecular weight (Mw) and number-average molecular weight (Mn) of each copolymer were measured using gel permeation chromatography (GPC) (GPC-8000 series produced by Tosoh Corporation, detector: differential refractometer, column: TSKGEL SUPERMULTIPORE HZ-M produced by Tosoh Corporation), and expressed relative to polystyrene standards. A molecular weight distribution Mw/Mn was calculated from the measurement results.

<Structural Identification of Copolymers>

Structures (styrene content, vinyl content) of copolymers were identified with a device of JNM-ECA series produced by JEOL Ltd. Each polymer (0.1 g) was dissolved in toluene (15 mL), and the solution was slowly introduced in methanol (30 mL) for reprecipitation. The resulting precipitate was dried under reduced pressure, and then measured.

<Synthesis of Copolymer (1)>

n-Hexane (18 L), styrene (600 g), butadiene (1400 g), the modifier (1) (40 mL), and TMEDA (10 mmol) were charged into a sufficiently nitrogen-purged 30-L pressure resistant container, and heated to 40° C. After further addition of the initiator (2) (34 mL), the mixture was heated to 50° C., and stirred for 3 hours. Next, the modifier (2) (20 mL) was added, followed by stirring for 30 minutes, and the reaction solution was mixed with methanol (15 mL) and 2,6-tert-butyl-p-cresol (0.1 g). Thereafter, a coagulum was recovered from the polymer solution by steam stripping treatment, and the coagulum was dried under reduced pressure for 24 hours to give a copolymer (1). Here, 0.32 g of the silicon-containing vinyl compound (modifier (1)) was added for each 100 g of the monomer component; 0.85 mmol of the polymerization initiator (initiator (2)) was added for each 100 g of the monomer component; and 1.18 mol of the compound (modifier (2)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (2)>

A copolymer (2) was produced based on the same formulation as that for synthesis of the copolymer (1), except that the initiator (3) (34 mL) was used instead of the initiator (2) (34 mL). Here, 0.32 g of the silicon-containing vinyl compound (modifier (1)) was added for each 100 g of the monomer component; 0.85 mmol of the polymerization initiator (initiator (3)) was added for each 100 g of the monomer component; and 1.18 mol of the compound (modifier (2)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (3)>

A copolymer (3) was produced based on the same formulation as that for synthesis of the copolymer (1), except that the amounts of styrene and butadiene were changed to 900 g and 1100 g, respectively. Here, 0.32 g of the silicon-containing vinyl compound (modifier (1)) was added for each 100 g of the monomer component; 0.85 mmol of the polymerization initiator (initiator (2)) was added for each 100 g of the monomer component; and 1.18 mol of the compound (modifier (2)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (4)>

A copolymer (4) was produced based on the same formulation as that for synthesis of the copolymer (1), except that the initiator (1) (19 mL) was used instead of the initiator (2) (34 mL). Here, 0.32 g of the silicon-containing vinyl compound (modifier (1)) was added for each 100 g of the monomer component; 0.85 mmol of the polymerization initiator (initiator (1)) was added for each 100 g of the monomer component; and 1.18 mol of the compound (modifier (2)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (5)>

n-Hexane (18 L), styrene (600 g), butadiene (1400 g), the modifier (1) (75 mL), and TMEDA (10 mmol) were charged into a sufficiently nitrogen-purged 30-L pressure resistant container, and heated to 40° C. After further addition of the initiator (1) (19 mL), the mixture was heated to 50° C. and stirred for 30 minutes. Further, the modifier (1) (75 mL) was added, and the mixture was stirred for 2.5 hours. Next, the modifier (2) (20 mL) was added, followed by stirring for 30 minutes, and the reaction solution was mixed with methanol (1 mL) and 2,6-tert-butyl-p-cresol (0.1 g). Thereafter, a coagulum was recovered from the polymer solution by steam stripping treatment, and the coagulum was dried under reduced pressure for 24 hours to give a copolymer (5). Here, 1.19 g of the silicon-containing vinyl compound (modifier (1)) was added for each 100 g of the monomer component; 0.85 mmol of the polymerization initiator (initiator (1)) was added for each 100 g of the monomer component; and 1.18 mol of the compound (modifier (2)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (6)>

A copolymer (6) was produced based on the same formulation as that for synthesis of the copolymer (4), except that the amounts of styrene and butadiene were changed to 0 g and 2000 g, respectively; THF (5 mmol) was used instead of TMEDA (10 mmol); and the initiator (1) (23 mL) was used instead of the initiator (1) (19 mL). Here, 0.32 g of the silicon-containing vinyl compound (modifier (1)) was added for each 100 g of the monomer component; 1.05 mmol of the polymerization initiator (initiator (1)) was added for each 100 g of the monomer component; and 0.95 mol of the compound (modifier (2)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (7)>

A copolymer (7) was produced based on the same formulation as that for synthesis of the copolymer (4), except that the modifier (3) (40 mL) was used instead of the modifier (1) (40 mL). Here, 0.43 g of the silicon-containing vinyl compound (modifier (3)) was added for each 100 g of the monomer component; 0.85 mmol of the polymerization initiator (initiator (1)) was added for each 100 g of the monomer component; and 1.18 mol of the compound (modifier (2)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (8)>

A copolymer (8) was produced based on the same formulation as that for synthesis of the copolymer (7), except that an n-butyllithium solution (10.6 mL) was used instead of the initiator (1) (19 mL). Here, 0.43 g of the silicon-containing vinyl compound (modifier (3)) was added for each 100 g of the monomer component; and 1.18 mol of the compound (modifier (2)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (9)>

A copolymer (9) was produced based on the same formulation as that for synthesis of the copolymer (6), except that an n-butyllithium solution (13 mL) was used instead of the initiator (1) (23 mL). Here, 0.43 g of the silicon-containing vinyl compound (modifier (1)) was added for each 100 g of the monomer component; and 0.95 mol of the compound (modifier (2)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (10)>

A copolymer (10) was produced based on the same formulation as that for synthesis of the copolymer (1), except that the amount of the modifier (1) was changed from 40 mL to 0 mL. Here, 0.85 mmol of the polymerization initiator (initiator (2)) was added for each 100 g of the monomer component; and 1.18 mol of the compound (modifier (2)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (11)>

A copolymer (11) was produced based on the same formulation as that for synthesis of the copolymer (1), except that the amount of the modifier (2) was changed from 20 mL to 0 mL. Here, 0.32 g of the silicon-containing vinyl compound (modifier (1)) was added for each 100 g of the monomer component; and 0.85 mmol of the polymerization initiator (initiator (2)) was added for each 100 g of the monomer component.

<Synthesis of Copolymer (12)>

n-Hexane (18 L), styrene (600 g), butadiene (1400 g), and TMEDA (10 mmol) were charged into a sufficiently nitrogen-purged 30-L pressure resistant container, and heated to 40° C. After further addition of an n-butyllithium solution (11 mL), the mixture was heated to 50° C. and stirred for 3 hours. Next, the reaction solution was mixed with methanol (1 mL) and 2,6-tert-butyl-p-cresol (0.1 g). A coagulum was recovered from the polymer solution by steam stripping treatment, and the coagulum was dried under reduced pressure for 24 hours to give a copolymer (12).

<Synthesis of Copolymer (13)>

A copolymer (13) was produced based on the same formulation as that for synthesis of the copolymer (7), except that a coagulum was recovered from the polymer solution not by steam stripping treatment but by evaporating the polymer solution at room temperatures for 24 hours, followed by drying the coagulum under reduced pressure. Here, 0.43 g of the silicon-containing vinyl compound (modifier (3)) was added for each 100 g of the monomer component; 0.85 mmol of the polymerization initiator (initiator (1)) was added for each 100 g of the monomer component; and 1.18 mol of the compound (modifier (2)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (14)>

A copolymer (14) was produced based on the same formulation as that for synthesis of the copolymer (7), except that the amounts of the modifier (3) (40 mL) and the modifier (2) (20 mL) were changed to 0 mL. Here, 8.5 mmol of the polymerization initiator (initiator (1)) was added for each 100 g of the monomer component.

<Synthesis of Copolymer (15)>

A copolymer (15) was produced based on the same formulation as that for synthesis of the copolymer (7), except that an n-butyllithium solution (6.8 mL) was used instead of the initiator (1) (19 mL), and the amount of the modifier (2) was changed from 20 mL to 0 mL. Here, 0.43 g of the silicon-containing vinyl compound (modifier (3)) was added for each 100 g of the monomer component.

<Synthesis of Copolymer (16)>

A copolymer (16) was produced based on the same formulation as that for synthesis of the copolymer (7), except that an n-butyllithium solution (6.8 mL) was used instead of the initiator (1) (19 mL); and the amount of the modifier (3) was changed from 40 mL to 0 mL. Here, 1.18 mol of the compound (modifier (2)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (17)>

A copolymer (17) was produced based on the same formulation as that for synthesis of the copolymer (1), except that the initiator (4) (bifunctional initiator, 68 mL) was used instead of the initiator (2) (34 mL); and the amount of the modifier (2) was changed from 20 mL to 40 mL. Here, 0.32 g of the silicon-containing vinyl compound (modifier (1)) was added for each 100 g of the monomer component; and 2.28 mol (1.14 mol for each terminal) of the compound (modifier (2)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (18)>

A copolymer (18) was produced based on the same formulation as that for synthesis of the copolymer (7), except that the amounts of styrene and butadiene were changed to 0 g and 2000 g, respectively; THF (5 mmol) was used instead of TMEDA (10 mmol); and the amount of the initiator (1) was changed from 19 mL to 23 mL). Here, 0.43 g of the silicon-containing vinyl compound (modifier (3)) was added for each 100 g of the monomer component; 0.85 mmol of the polymerization initiator (initiator (1)) was added for each 100 g of the monomer component; and 1.18 mol of the compound (modifier (2)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (19)>

A copolymer (19) was produced based on the same formulation as that for synthesis of the copolymer (8), except that the amounts of styrene and butadiene were changed to 0 g and 2000 g, respectively; and THF (5 mmol) was used instead of TMEDA (10 mmol). Here, 0.43 g of the silicon-containing vinyl compound (modifier (3)) was added for each 100 g of the monomer component; and 1.18 mol of the compound (modifier (2)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (20)>

n-Hexane (18 L), butadiene (2000 g), and THF (5 mmol) were charged into a sufficiently nitrogen-purged 30-L pressure resistant container, and heated to 40° C. After further addition of an n-butyllithium solution (11 mL), the mixture was heated to 50° C., and stirred for 3 hours. Next, the reaction solution was mixed with methanol (1 mL) and 2,6-tert-butyl-p-cresol (0.1 g). Then, a coagulum was recovered from the polymer solution by steam stripping treatment, and the coagulum was dried under reduced pressure for 24 hours to give a copolymer (20).

<Synthesis of Copolymer (21)>

A copolymer (21) was produced based on the same formulation as that for synthesis of the copolymer (18), except that a coagulum was recovered from the polymer solution not by steam stripping treatment but by evaporating the polymer solution at room temperatures for 24 hours, followed by drying the coagulum under reduced pressure. Here, 0.43 g of the silicon-containing vinyl compound (modifier (3)) was added for each 100 g of the monomer component; 0.85 mmol of the polymerization initiator (initiator (1)) was added for each 100 g of the monomer component; and 1.18 mol of the compound (modifier (2)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (22)>

A copolymer (22) was produced based on the same formulation as that for synthesis of the copolymer (1), except that the modifier (4) (20 mL) was used instead of the modifier (2) (20 mL). Here, 0.32 g of the silicon-containing vinyl compound (modifier (1)) was added for each 100 g of the monomer component; 0.85 mmol of the polymerization initiator (initiator (2)) was added for each 100 g of the monomer component; and 1.18 mol of the compound (modifier (4)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (23)>

A copolymer (23) was produced based on the same formulation as that for synthesis of the copolymer (2), except that the modifier (4) (20 mL) was used instead of the modifier (2) (20 mL). Here, 0.32 g of the silicon-containing vinyl compound (modifier (1)) was added for each 100 g of the monomer component; 0.85 mmol of the polymerization initiator (initiator (3)) was added for each 100 g of the monomer component; and 1.18 mol of the compound (modifier (4)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (24)>

A copolymer (24) was produced based on the same formulation as that for synthesis of the copolymer (3), except that the modifier (4) (20 mL) was used instead of the modifier (2) (20 mL). Here, 0.32 g of the silicon-containing vinyl compound (modifier (1)) was added for each 100 g of the monomer component; 0.85 mmol of the polymerization initiator (initiator (2)) was added for each 100 g of the monomer component; and 1.18 mol of the compound (modifier (4)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (25)>

A copolymer (25) was produced based on the same formulation as that for synthesis of the copolymer (4), except that the modifier (4) (20 mL) was used instead of the modifier (2) (20 mL). Here, 0.32 g of the silicon-containing vinyl compound (modifier (1)) was added for each 100 g of the monomer component; 0.85 mmol of the polymerization initiator (initiator (1)) was added for each 100 g of the monomer component; and 1.18 mol of the compound (modifier (4)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (26)>

A copolymer (26) was produced based on the same formulation as that for synthesis of the copolymer (5), except that the modifier (4) (20 mL) was used instead of the modifier (2) (20 mL). Here, 1.19 g of the silicon-containing vinyl compound (modifier (1)) was added for each 100 g of the monomer component; 0.85 mmol of the polymerization initiator (initiator (1)) was added for each 100 g of the monomer component; and 1.18 mol of the compound (modifier (4)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (27)>

A copolymer (27) was produced based on the same formulation as that for synthesis of the copolymer (6), except that the modifier (4) (20 mL) was used instead of the modifier (2) (20 mL). Here, 0.32 g of the silicon-containing vinyl compound (modifier (1)) was added for each 100 g of the monomer component; 1.05 mmol of the polymerization initiator (initiator (1)) was added for each 100 g of the monomer component; and 0.95 mol of the compound (modifier (4)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (28)>

A copolymer (28) was produced based on the same formulation as that for synthesis of the copolymer (7), except that the modifier (4) (20 mL) was used instead of the modifier (2) (20 mL). Here, 0.32 g of the silicon-containing vinyl compound (modifier (3)) was added for each 100 g of the monomer component; 0.85 mmol of the polymerization initiator (initiator (1)) was added for each 100 g of the monomer component; and 1.18 mol of the compound (modifier (4)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (29)>

A copolymer (29) was produced based on the same formulation as that for synthesis of the copolymer (28), except that a coagulum was recovered from the polymer solution not by steam stripping treatment but by evaporating the polymer solution at room temperatures for 24 hours, followed by drying the coagulum under reduced pressure. Here, 0.32 g of the silicon-containing vinyl compound (modifier (3)) was added for each 100 g of the monomer component; 0.85 mmol of the polymerization initiator (initiator (1)) was added for each 100 g of the monomer component; and 1.18 mol of the compound (modifier (4)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (30)>

A copolymer (30) was produced based on the same formulation as that for synthesis of the copolymer (28), except that an n-butyllithium solution (10.6 mL) was used instead of the initiator (1) (19 mL); and the amount of the modifier (3) was changed from 40 mL to 0 mL. Here, 1.18 mol of the compound (modifier (4)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (31)>

A copolymer (31) was produced based on the same formulation as that for synthesis of the copolymer (18), except that the modifier (4) (20 mL) was used instead of the modifier (2) (20 mL). Here, 0.32 g of the silicon-containing vinyl compound (modifier (3)) was added for each 100 g of the monomer component; 0.85 mmol of the polymerization initiator (initiator (1)) was added for each 100 g of the monomer component; and 1.18 mol of the compound (modifier (4)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (32)>

A copolymer (32) was produced based on the same formulation as that for synthesis of the copolymer (31), except that a coagulum was recovered from the polymer solution not by steam stripping treatment but by evaporating the polymer solution at room temperatures for 24 hours, followed by drying the coagulum under reduced pressure. Here, 0.32 g of the silicon-containing vinyl compound (modifier (3)) was added for each 100 g of the monomer component; 0.85 mmol of the polymerization initiator (initiator (1)) was added for each 100 g of the monomer component; and 1.18 mol of the compound (modifier (4)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (33)>

A copolymer (33) was produced based on the same formulation as that for synthesis of the copolymer (1), except that the modifier (5) (20 mL) was used instead of the modifier (2) (20 mL). Here, 0.32 g of the silicon-containing vinyl compound (modifier (1)) was added for each 100 g of the monomer component; 0.85 mmol of the polymerization initiator (initiator (2)) was added for each 100 g of the monomer component; and 1.18 mol of the compound (modifier (5)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (34)>

A copolymer (34) was produced based on the same formulation as that for synthesis of the copolymer (2), except that the modifier (5) (20 mL) was used instead of the modifier (2) (20 mL). Here, 0.32 g of the silicon-containing vinyl compound (modifier (1)) was added for each 100 g of the monomer component; 0.85 mmol of the polymerization initiator (initiator (3)) was added for each 100 g of the monomer component; and 1.18 mol of the compound (modifier (5)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (35)>

A copolymer (35) was produced based on the same formulation as that for synthesis of the copolymer (3), except that the modifier (5) (20 mL) was used instead of the modifier (2) (20 mL). Here, 0.32 g of the silicon-containing vinyl compound (modifier (1)) was added for each 100 g of the monomer component; 0.85 mmol of the polymerization initiator (initiator (2)) was added for each 100 g of the monomer component; and 1.18 mol of the compound (modifier (5)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (36)>

A copolymer (36) was produced based on the same formulation as that for synthesis of the copolymer (4), except that the modifier (5) (20 mL) was used instead of the modifier (2) (20 mL). Here, 0.32 g of the silicon-containing vinyl compound (modifier (1)) was added for each 100 g of the monomer component; 0.85 mmol of the polymerization initiator (initiator (1)) was added for each 100 g of the monomer component; and 1.18 mol of the compound (modifier (5)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (37)>

A copolymer (37) was produced based on the same formulation as that for synthesis of the copolymer (5), except that the modifier (5) (20 mL) was used instead of the modifier (2) (20 mL). Here, 1.19 g of the silicon-containing vinyl compound (modifier (1)) was added for each 100 g of the monomer component; 0.85 mmol of the polymerization initiator (initiator (1)) was added for each 100 g of the monomer component; and 1.18 mol of the compound (modifier (5)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (38)>

A copolymer (38) was produced based on the same formulation as that for synthesis of the copolymer (7), except that the modifier (5) (20 mL) was used instead of the modifier (2) (20 mL). Here, 0.32 g of the silicon-containing vinyl compound (modifier (3)) was added for each 100 g of the monomer component; 0.85 mmol of the polymerization initiator (initiator (1)) was added for each 100 g of the monomer component; and 1.18 mol of the compound (modifier (5)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (39)>

A copolymer (39) was produced based on the same formulation as that for synthesis of the copolymer (38), except that a coagulum was recovered from the polymer solution not by steam stripping treatment but by evaporating the polymer solution at room temperatures for 24 hours, followed by drying the coagulum under reduced pressure. Here, 0.32 g of the silicon-containing vinyl compound (modifier (3)) was added for each 100 g of the monomer component; 0.85 mmol of the polymerization initiator (initiator (1)) was added for each 100 g of the monomer component; and 1.18 mol of the compound (modifier (5)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (40)>

A copolymer (40) was produced based on the same formulation as that for synthesis of the copolymer (7), except that the modifier (6) (20 mL) was used instead of the modifier (2) (20 mL). Here, 0.32 g of the silicon-containing vinyl compound (modifier (3)) was added for each 100 g of the monomer component; 0.85 mmol of the polymerization initiator (initiator (1)) was added for each 100 g of the monomer component; and 1.18 mol of the compound (modifier (6)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (41)>

A copolymer (41) was produced based on the same formulation as that for synthesis of the copolymer (7), except that the modifier (7) (20 mL) was used instead of the modifier (2) (20 mL). Here, 0.32 g of the silicon-containing vinyl compound (modifier (3)) was added for each 100 g of the monomer component; 0.85 mmol of the polymerization initiator (initiator (1)) was added for each 100 g of the monomer component; and 1.18 mol of the compound (modifier (7)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (42)>

A copolymer (42) was produced based on the same formulation as that for synthesis of the copolymer (38), except that a butyllithium solution (10.6 mL) was used instead of the initiator (1) (19 mL), and the amount of the modifier (3) was changed from 40 mL to 0 mL. Here, 1.18 mol of the compound (modifier (5)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (43)>

A copolymer (43) was produced based on the same formulation as that for synthesis of the copolymer (1), except that the modifier (8) (20 mL) was used instead of the modifier (2) (20 mL). Here, 0.32 g of the silicon-containing vinyl compound (modifier (1)) was added for each 100 g of the monomer component; 0.85 mmol of the polymerization initiator (initiator (2)) was added for each 100 g of the monomer component; and 1.18 mol of the compound (modifier (8)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (44)>

A copolymer (44) was produced based on the same formulation as that for synthesis of the copolymer (2), except that the modifier (8) (20 mL) was used instead of the modifier (2) (20 mL). Here, 0.32 g of the silicon-containing vinyl compound (modifier (1)) was added for each 100 g of the monomer component; 0.85 mmol of the polymerization initiator (initiator (3)) was added for each 100 g of the monomer component; and 1.18 mol of the compound (modifier (8)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (45)>

A copolymer (45) was produced based on the same formulation as that for synthesis of the copolymer (3), except that the modifier (8) (20 mL) was used instead of the modifier (2) (20 mL). Here, 0.32 g of the silicon-containing vinyl compound (modifier (1)) was added for each 100 g of the monomer component; 0.85 mmol of the polymerization initiator (initiator (2)) was added for each 100 g of the monomer component; and 1.18 mol of the compound (modifier (8)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (46)>

A copolymer (46) was produced based on the same formulation as that for synthesis of the copolymer (4), except that the modifier (8) (20 mL) was used instead of the modifier (2) (20 mL). Here, 0.32 g of the silicon-containing vinyl compound (modifier (1)) was added for each 100 g of the monomer component; 0.85 mmol of the polymerization initiator (initiator (1)) was added for each 100 g of the monomer component; and 1.18 mol of the compound (modifier (8)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (47)>

A copolymer (47) was produced based on the same formulation as that for synthesis of the copolymer (5), except that the modifier (8) (20 mL) was used instead of the modifier (2) (20 mL). Here, 1.19 g of the silicon-containing vinyl compound (modifier (1)) was added for each 100 g of the monomer component; 0.85 mmol of the polymerization initiator (initiator (1)) was added for each 100 g of the monomer component; and 1.18 mol of the compound (modifier (8)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (48)>

A copolymer (48) was produced based on the same formulation as that for synthesis of the copolymer (7), except that the modifier (8) (20 mL) was used instead of the modifier (2) (20 mL). Here, 0.32 g of the silicon-containing vinyl compound (modifier (3)) was added for each 100 g of the monomer component; 0.85 mmol of the polymerization initiator (initiator (1)) was added for each 100 g of the monomer component; and 1.18 mol of the compound (modifier (8)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (49)>

A copolymer (49) was produced based on the same formulation as that for synthesis of the copolymer (48), except that a butyllithium solution (10.6 mL) was used instead of the initiator (1) (19 mL), and the amount of the modifier (3) was changed from 40 mL to 0 mL. Here, 1.18 mol of the compound (modifier (8)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (50)>

A copolymer (50) was produced based on the same formulation as that for synthesis of the copolymer (1), except that the modifier (9) (20 mL) was used instead of the modifier (2) (20 mL). Here, 0.32 g of the silicon-containing vinyl compound (modifier (1)) was added for each 100 g of the monomer component; 0.85 mmol of the polymerization initiator (initiator (2)) was added for each 100 g of the monomer component; and 1.18 mol of the compound (modifier (9)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (51)>

A copolymer (51) was produced based on the same formulation as that for synthesis of the copolymer (2), except that the modifier (9) (20 mL) was used instead of the modifier (2) (20 mL). Here, 0.32 g of the silicon-containing vinyl compound (modifier (1)) was added for each 100 g of the monomer component; 0.85 mmol of the polymerization initiator (initiator (3)) was added for each 100 g of the monomer component; and 1.18 mol of the compound (modifier (9)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (52)>

A copolymer (52) was produced based on the same formulation as that for synthesis of the copolymer (3), except that the modifier (9) (20 mL) was used instead of the modifier (2) (20 mL). Here, 0.32 g of the silicon-containing vinyl compound (modifier (1)) was added for each 100 g of the monomer component; 0.85 mmol of the polymerization initiator (initiator (2)) was added for each 100 g of the monomer component; and 1.18 mol of the compound (modifier (9)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (53)>

A copolymer (53) was produced based on the same formulation as that for synthesis of the copolymer (4), except that the modifier (9) (20 mL) was used instead of the modifier (2) (20 mL). Here, 0.32 g of the silicon-containing vinyl compound (modifier (1)) was added for each 100 g of the monomer component; 0.85 mmol of the polymerization initiator (initiator (1)) was added for each 100 g of the monomer component; and 1.18 mol of the compound (modifier (9)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (54)>

A copolymer (54) was produced based on the same formulation as that for synthesis of the copolymer (5), except that the modifier (9) (20 mL) was used instead of the modifier (2) (20 mL). Here, 1.19 g of the silicon-containing vinyl compound (modifier (1)) was added for each 100 g of the monomer component; 0.85 mmol of the polymerization initiator (initiator (1)) was added for each 100 g of the monomer component; and 1.18 mol of the compound (modifier (9)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (55)>

A copolymer (55) was produced based on the same formulation as that for synthesis of the copolymer (7), except that the modifier (9) (20 mL) was used instead of the modifier (2) (20 mL). Here, 0.32 g of the silicon-containing vinyl compound (modifier (3)) was added for each 100 g of the monomer component; 0.85 mmol of the polymerization initiator (initiator (1)) was added for each 100 g of the monomer component; and 1.18 mol of the compound (modifier (9)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

<Synthesis of Copolymer (56)>

A copolymer (56) was produced based on the same formulation as that for synthesis of the copolymer (55), except that a butyllithium solution (10.6 mL) was used instead of the initiator (1) (19 mL), and the amount of the modifier (3) was changed from 40 mL to 0 mL. Here, 1.18 mol of the compound (modifier (9)) containing a nitrogen atom and/or a silicon atom was added per mol of the alkali metal derived from the polymerization initiator added.

Tables 1 to 5 summarize the monomer components and others of the copolymers (1) to (56).

TABLE 1
Examples in which a compound represented by the formula (IIId) is used as a Terminal modifier
						Molecular	Molecular
				Styrene	Vinyl	weight	weight
			Terminal	content	content	distribution	Mw (unit:
Copolymer	Initiator	Monomer component	modifier	(% by mass)	(mol %)	Mw/Mn	ten thousand)
Copolymer (1)	Initiator (2)	Styrene, 1,3-Butadiene, Modifier (1)	Modifier (2)	30	56	1.21	26.5
Copolymer (2)	Initiator (3)	Styrene, 1,3-Butadiene, Modifier (1)	Modifier (2)	30	57	1.23	26.8
Copolymer (3)	Initiator (2)	Styrene, 1,3-Butadiene, Modifier (1)	Modifier (2)	45	56	1.23	26.9
Copolymer (4)	Initiator (1)	Styrene, 1,3-Butadiene, Modifier (1)	Modifier (2)	30	56	1.13	24.8
Copolymer (5)	Initiator (1)	Styrene, 1,3-Butadiene, Modifier (1)	Modifier (2)	30	56	1.20	27.1
Copolymer (6)	Initiator (1)	1,3-Butadiene, Modifier (1)	Modifier (2)	0	14.2	1.17	28.9
Copolymer (7)	Initiator (1)	Styrene, 1,3-Butadiene, Modifier (3)	Modifier (2)	30	56	1.18	26.0
Copolymer (8)	n-Butyllithium solution	Styrene, 1,3-Butadiene, Modifier (3)	Modifier (2)	30	55	1.17	24.5
Copolymer (9)	n-Butyllithium solution	1,3-Butadiene, Modifier (1)	Modifier (2)	0	13.5	1.16	29.3
Copolymer (10)	Initiator (2)	Styrene, 1,3-Butadiene	Modifier (2)	30	56	1.19	25.0
Copolymer (11)	Initiator (2)	Styrene, 1,3-Butadiene, Modifier (1)	Not added	30	56	1.25	25.4
Copolymer (12)	n-Butyllithium solution	Styrene, 1,3-Butadiene	Not added	30	56	1.09	26.5
Copolymer (13)	Initiator (1)	Styrene, 1,3-Butadiene, Modifier (3)	Modifier (2)	30	57	1.19	25.2
Copolymer (14)	Initiator (1)	Styrene, 1,3-Butadiene	Not added	30	57	1.16	26.1
Copolymer (15)	n-Butyllithium solution	Styrene, 1,3-Butadiene, Modifier (3)	Not added	30	56	1.13	27.9
Copolymer (16)	n-Butyllithium solution	Styrene, 1,3-Butadiene	Modifier (2)	30	55	1.10	27.4
Copolymer (17)	Initiator (4)	Styrene, 1,3-Butadiene, Modifier (1)	Modifier (2)	30	55	1.29	28.9
Copolymer (18)	Initiator (1)	1,3-Butadiene, Modifier (3)	Modifier (2)	0	14.2	1.19	26.2
Copolymer (19)	n-Butyllithium solution	1,3-Butadiene, Modifier (3)	Modifier (2)	0	13.7	1.16	25.2
Copolymer (20)	n-Butyllithium solution	1,3-Butadiene	Not added	0	13.9	1.11	27.1
Copolymer (21)	Initiator (1)	1,3-Butadiene, Modifier (3)	Modifier (2)	0	14	1.21	26.3

TABLE 2
Examples in which a compound represented by the formula (IV) is used as a Terminal modifier
						Molecular	Molecular
				Styrene	Vinyl	weight	weight
			Terminal	content	content	distribution	Mw (unit:
Copolymer	Initiator	Monomer component	modifier	(% by mass)	(mol %)	Mw/Mn	ten thousand)
Copolymer (22)	Initiator (2)	Styrene, 1,3-Butadiene, Modifier (1)	Modifier (4)	30	57	1.26	28.3
Copolymer (23)	Initiator (3)	Styrene, 1,3-Butadiene, Modifier (1)	Modifier (4)	30	57	1.28	28.0
Copolymer (24)	Initiator (2)	Styrene, 1,3-Butadiene, Modifier (1)	Modifier (4)	45	56	1.25	29.2
Copolymer (25)	Initiator (1)	Styrene, 1,3-Butadiene, Modifier (1)	Modifier (4)	30	56	1.19	27.2
Copolymer (26)	Initiator (1)	Styrene, 1,3-Butadiene, Modifier (1)	Modifier (4)	30	57	1.17	26.1
Copolymer (27)	Initiator (1)	1,3-Butadiene, Modifier (1)	Modifier (4)	0	13.9	1.17	25.9
Copolymer (28)	Initiator (1)	Styrene, 1,3-Butadiene, Modifier (3)	Modifier (4)	30	56	1.20	25.8
Copolymer (29)	Initiator (1)	Styrene, 1,3-Butadiene, Modifier (3)	Modifier (4)	30	58	1.18	26.2
Copolymer (30)	n-Butyllithium solution	Styrene, 1,3-Butadiene	Modifier (4)	30	56	1.14	27.1
Copolymer (31)	Initiator (1)	1,3-Butadiene, Modifier (3)	Modifier (4)	0	14.1	1.21	26.2
Copolymer (32)	Initiator (1)	1,3-Butadiene, Modifier (3)	Modifier (4)	0	14.2	1.18	26.8

TABLE 3
Examples in which a compound represented by the formula (IIIb) is used as a Terminal modifier
						Molecular	Molecular
				Styrene	Vinyl	weight	weight
			Terminal	content	content	distribution	Mw (unit:
Copolymer	Initiator	Monomer component	modifier	(% by mass)	(mol %)	Mw/Mn	ten thousand)
Copolymer (33)	Initiator (2)	Styrene, 1,3-Butadiene, Modifier (1)	Modifier (5)	30	57	1.18	27.1
Copolymer (34)	Initiator (3)	Styrene, 1,3-Butadiene, Modifier (1)	Modifier (5)	30	56	1.16	26.3
Copolymer (35)	Initiator (2)	Styrene, 1,3-Butadiene, Modifier (1)	Modifier (5)	45	56	1.16	24.6
Copolymer (36)	Initiator (1)	Styrene, 1,3-Butadiene, Modifier (1)	Modifier (5)	30	57	1.12	24.9
Copolymer (37)	Initiator (1)	Styrene, 1,3-Butadiene, Modifier (1)	Modifier (5)	30	56	1.13	26.7
Copolymer (38)	Initiator (1)	Styrene, 1,3-Butadiene, Modifier (3)	Modifier (5)	30	56	1.13	25.6
Copolymer (39)	Initiator (1)	Styrene, 1,3-Butadiene, Modifier (3)	Modifier (5)	30	56	1.10	25.5
Copolymer (40)	Initiator (1)	Styrene, 1,3-Butadiene, Modifier (3)	Modifier (6)	30	57	1.14	252
Copolymer (41)	Initiator (1)	Styrene, 1,3-Butadiene, Modifier (3)	Modifier (7)	30	56	1.15	25.9
Copolymer (42)	n-Butyllithium solution	Styrene, 1,3-Butadiene	Modifier (5)	30	55	1.09	26.3

TABLE 4
Examples in which a compound containing an alkoxysilyl group, a nitrogen atom and a carbonyl group is used as a Terminal modifier
						Molecular	Molecular
				Styrene	Vinyl	weight	weight
			Terminal	content	content	distribution	Mw (unit:
Copolymer	Initiator	Monomer component	modifier	(% by mass)	(mol %)	Mw/Mn	ten thousand)
Copolymer (43)	Initiator (2)	Styrene, 1,3-Butadiene, Modifier (1)	Modifier (8)	30	56	1.24	27.5
Copolymer (44)	Initiator (3)	Styrene, 1,3-Butadiene, Modifier (1)	Modifier (8)	30	56	1.22	28.3
Copolymer (45)	Initiator (2)	Styrene, 1,3-Butadiene, Modifier (1)	Modifier (8)	45	57	1.23	27.8
Copolymer (46)	Initiator (1)	Styrene, 1,3-Butadiene, Modifier (1)	Modifier (8)	30	56	1.20	28.5
Copolymer (47)	Initiator (1)	Styrene, 1,3-Butadiene, Modifier (1)	Modifier (8)	30	55	1.19	28.6
Copolymer (48)	Initiator (1)	Styrene, 1,3-Butadiene, Modifier (3)	Modifier (8)	30	56	1.22	28.3
Copolymer (49)	n-Butyllithium solution	Styrene, 1,3-Butadiene	Modifier (8)	30	56	1.16	27.3

TABLE 5
Examples in which an N,N-dialkyl-substituted carboxylic acid amide dialkyl acetal compound is used as a Terminal modifier
						Molecular	Molecular
				Styrene	Vinyl	weight	weight
			Terminal	content	content	distribution	Mw (unit:
Copolymer	Initiator	Monomer component	modifier	(% by mass)	(mol %)	Mw/Mn	ten thousand)
Copolymer (50)	Initiator (2)	Styrene, 1,3-Butadiene, Modifier (1)	Modifier (9)	30	57	1.20	27.2
Copolymer (51)	Initiator (3)	Styrene, 1,3-Butadiene, Modifier (1)	Modifier (9)	30	56	1.21	27.3
Copolymer (52)	Initiator (2)	Styrene, 1,3-Butadiene, Modifier (1)	Modifier (9)	45	55	1.21	27.8
Copolymer (53)	Initiator (1)	Styrene, 1,3-Butadiene, Modifier (1)	Modifier (9)	30	56	1.20	27.6
Copolymer (54)	Initiator (1)	Styrene, 1,3-Butadiene, Modifier (1)	Modifier (9)	30	56	1.19	26.9
Copolymer (55)	Initiator (1)	Styrene, 1,3-Butadiene, Modifier (3)	Modifier (9)	30	57	1.18	26.8
Copolymer (56)	n-Butyllithium solution	Styrene, 1,3-Butadiene	Modifier (9)	30	57	1.17	27.1

The following describes the various chemicals used in the examples and comparative examples.

Copolymers (1) to (56): synthesized as above

Natural Rubber: TSR20

Polybutadiene rubber: Ubepol BR150B produced by Ube Industries, Ltd.

Silica 1: ZEOSIL 1085GR produced by Rhodia (nitrogen adsorption specific surface area: 80 m²/g)

Silica 2: ZEOSIL 115GR produced by Rhodia (nitrogen adsorption specific surface area: 110 m²/g)

Silica 3: ZEOSIL 1165 MP produced by Rhodia (nitrogen adsorption specific surface area: 160 m²/g)

Silica 4: ZEOSIL 1205 MP produced by Rhodia (nitrogen adsorption specific surface area: 200 m²/g)

Silane coupling agent A: Si69 (bis(3-triethoxysilylpropyl)tetrasulfide) produced by Evonik Degussa

Silane coupling agent B: Si363 produced by Evonik Degussa

Silane coupling agent C: NXT-Z45 (a compound containing linking unit A and linking unit B (linking unit A: 55 mol %, linking unit B: 45 mol %)) produced by Momentive Performance Materials

Carbon black: Diablack N339 (N₂SA: 96 m²/g, DBP absorption: 124 mL/100 g) produced by Mitsubishi Chemical Corporation

Coumarone indene resin 1 (solid resin): NOVARES C90 (Tg: 90° C.) produced by Rutgers chemicals AG

Coumarone indene resin 2 (liquid resin): NOVARES C30 (Tg: 10° C.) produced by Rutgers chemicals AG

Coumarone indene resin 3 (liquid resin): NOVARES C10 (Tg: −30° C.) produced by Rutgers chemicals AG

α-Methylstyrene resin (copolymer of α-methyl styrene and styrene, solid resin): SYLVARES SA8.5 (Tg: 95° C.) produced by Arizona Chemical

Oil: X-140 produced by JX Nippon Oil & Energy Corporation

Antioxidant: Antigene 3C produced by Sumitomo Chemical Co., Ltd.

Stearic acid: TSUBAKI stearic acid beads produced by NOF Corporation

Zinc oxide: Zinc oxide #1 produced by Mitsui Mining & Smelting Co., Ltd.

Wax: Sunnoc N produced by Ouchi Shinko Chemical Industrial Co., Ltd.

Sulfur: sulfur powder produced by Tsurumi Chemical Industry Co., Ltd.

Vulcanization accelerator 1: Soxinol CZ produced by Sumitomo Chemical Co., Ltd.

Vulcanization accelerator 2: Soxinol D produced by Sumitomo Chemical Co., Ltd.

EXAMPLES AND COMPARATIVE EXAMPLES

According to each of the formulations shown in Tables 6 to 25, the materials other than the sulfur and vulcanization accelerators were kneaded for 5 minutes at 150° C. using a 1.7-L Banbury mixer (produced by Kobe Steel, Ltd.) to give a kneadate. The sulfur and vulcanization accelerators were then added to the kneadate, followed by kneading for 5 minutes at 80° C. using an open roll mill to give an unvulcanized rubber composition. The unvulcanized rubber composition was press-vulcanized for 20 minutes at 170° C. in a 0.5 mm-thick mold to obtain a vulcanized rubber composition.

Separately, the unvulcanized rubber composition was formed into a tread shape and assembled with other tire components on a tire building machine to form an unvulcanized tire. The unvulcanized tire was vulcanized for 12 minutes at 170° C. to prepare a test tire (size: 195/65R15).

<Evaluation Items and Test Methods>

In the evaluations below, Comparative Example 1 was considered as a standard comparative example in Tables 6 to 13; Comparative Example 22 was considered as a standard comparative example in Tables 14 to 19; and Comparative Example 40 was considered as a standard comparative example in Tables 20 to 25.

<Mixing and Kneading Processability Index>

The Mooney viscosity (ML₁₊₄/130° C.) of each unvulcanized rubber composition was determined in accordance with JIS K6300-1:2001 “Rubber, unvulcanized—Physical property—Part 1: Determination of Mooney viscosity and pre-vulcanization characteristics with Mooney viscometer” using a Mooney viscosity tester. That is, under a temperature condition of 130° C. achieved by 1 minute pre-heating, the Mooney viscosity of the unvulcanized rubber composition was measured after a small rotor was rotated for 4 minutes. The result is expressed as an index. A larger value indicates a lower Mooney viscosity, which in turn indicates better mixing and kneading processability. The index was calculated based on the following equation.
(Mixing and kneading processability index)=(Mooney viscosity of standard comparative example)/(Mooney viscosity of each formulation)×100
<Low-Heat-Build-Up Property>

The tan δ of each vulcanized rubber composition was measured at a dynamic strain amplitude of 1%, a frequency of 10 Hz, and at a temperature of 50° C. using a spectrometer (produced by Ueshima Seisakusho Co., Ltd.). The reciprocal value of the tan δ is expressed as an index relative to that of a standard comparative example (regarded as 100). A larger index indicates a smaller rolling resistance (less heat build-up), which in turn indicates better fuel economy.

<Tan δ Peak Temperature>

The tan δ of each vulcanized rubber composition was measured at a dynamic strain amplitude of 1%, a frequency of 10 Hz, a rate of temperature rise of 2° C./min., and at a measurement temperature ranging from −80 to 80° C. using a spectrometer (produced by Ueshima Seisakusho Co., Ltd.). The temperature at which tan δ reached its peak was determined as a tan δ peak temperature.

<Rubber Strength Index>

Each sample was subjected to a tensile test in accordance with JIS K 6251:2010 to measure the elongation at break. The measurement result was expressed as an index relative to the result of a standard comparative example (regarded as 100). A larger index indicates larger rubber strength (tensile strength).
(Rubber strength index)=(Elongation at break of each formulation)/(Elongation at break of Comparative Example 1)×100
<Abrasion Resistance Index>

The volume loss of each vulcanized rubber composition was measured with a laboratory abrasion and skid tester (LAT tester) at a load of 50 N, a speed of 20 km/h, and a slip angle of 5 degrees. The values (abrasion resistance index) in Tables 6 to 25 are relative values to the volume loss in the standard comparative example regarded as 100. A larger value indicates better abrasion resistance.

<Wet-Grip Performance Index>

The test tires of each example were mounted on all the wheels of a vehicle (front-engine, front-wheel drive (FF) vehicle, 2000 cc, made in Japan). The braking distance from an initial speed of 100 km/h was determined on a wet asphalt road surface. The result is expressed as an index. A larger index indicates better wet-skid performance (wet-grip performance). The index was calculated based on the following equation.
(Wet-grip performance index)=(Braking distance in standard comparative example)/(Braking distance of each formulation)×100
<Handling Stability>

The test tires of each example were mounted on all the wheels of a front-engine, front-wheel drive (FF) vehicle (2000 cc, made in Japan), and the vehicle was driven on a test course (dry road surface). The handling stability was evaluated based on sensory evaluation by a driver. The evaluation was scored on a scale of 1 to 10 relative to the evaluation of the standard comparative example being given 6. A higher score indicates better handling stability.

TABLE 6
Examples in which a compound represented by the formula (IIId) is used as a Terminal modifier
		Example
		1	2	3	4	5	6	7	8	9	10
Formulation	Copolymer (1)	65	—	—	—	—	—	—	—	—	—
(parts by mass)	Copolymer (2)	—	65	—	—	—	—	—	—	—	—
	Copolymer (3)	—	—	65	—	—	—	—	—	—	—
	Copolymer (4)	—	—	—	65	—	—	—	—	—	—
	Copolymer (5)	—	—	—	—	65	—	—	—	—	—
	Copolymer (6)	—	—	—	—	—	—	—	15	—	—
	Copolymer (7)	—	—	—	—	—	65	—	—	—	—
	Copolymer (8)	—	—	—	—	—	—	—	65	65	65
	Copolymer (9)	—	—	—	—	—	—	—	—	—	—
	Copolymer (10)	—	—	—	—	—	—	—	—	—	—
	Copolymer (11)	—	—	—	—	—	—	—	—	—	—
	Copolymer (12)	—	—	—	—	—	—	—	—	—	—
	Copolymer (13)	—	—	—	—	—	—	65	—	—	—
	Copolymer (14)	—	—	—	—	—	—	—	—	—	—
	Copolymer (15)	—	—	—	—	—	—	—	—	—	—
	Copolymer (16)	—	—	—	—	—	—	—	—	—	—
	Copolymer (17)	—	—	—	—	—	—	—	—	—	—
	Copolymer (18)	—	—	—	—	—	—	—	—	15	—
	Copolymer (19)	—	—	—	—	—	—	—	—	—	—
	Copolymer (20)	—	—	—	—	—	—	—	—	—	—
	Copolymer (21)	—	—	—	—	—	—	—	—	—	15
	Natural rubber	20	20	20	20	20	20	20	20	20	20
	Polybutadiene rubber	15	15	15	15	15	15	15	—	—	—
	Silica 2 (N2SA:	75	75	75	75	75	75	75	75	75	75
	110 m2/g)
	Silane coupling agent A	6	6	6	6	6	6	6	6	6	6
	Carbon black	5	5	5	5	5	5	5	5	5	5
	Oil	20	20	20	20	20	20	20	20	20	20
	Antioxidant	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5
	Stearic acid	2	2	2	2	2	2	2	2	2	2
	Zinc oxide	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5
	Wax	1	1	1	1	1	1	1	1	1	1
	Sulfur	2	2	2	2	2	2	2	2	2	2
	Vulcanization	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8
	accelerator 1
	Vulcanization	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2
	accelerator 2
Evaluation	Mixing and kneading	104	105	102	110	100	101	105	100	100	103
	processability index
	Low-heat-build-up	130	132	131	144	141	143	113	130	135	115
	property index
	tan δ peak temperature	−15	−15	−15	−15	−15	−15	−15	−15	−15	−15
	Rubber strength index	102	103	104	101	100	100	103	100	100	101
	Abrasion resistance	103	104	103	101	102	104	103	102	104	100
	index
	Wet-grip performance	113	113	112	111	111	114	109	108	109	107
	index
	Handling stability	6.25	6.25	6.25	6.25	6.25	6.25	6.25	6	6	6
		Comparative Example
		1	2	3	4	5	6	7	8	9	10	11
Formulation	Copolymer (1)	—	—	—	—	—	—	—	—	—	—	—
(parts by mass)	Copolymer (2)	—	—	—	—	—	—	—	—	—	—	—
	Copolymer (3)	—	—	—	—	—	—	—	—	—	—	—
	Copolymer (4)	—	—	—	—	—	—	—	—	—	—	—
	Copolymer (5)	—	—	—	—	—	—	—	—	—	—	—
	Copolymer (6)	—	—	—	—	—	—	—	—	—	—	—
	Copolymer (7)	—	—	—	—	—	—	—	—	—	—	—
	Copolymer (8)	65	—	—	—	—	—	—	—	65	65	65
	Copolymer (9)	—	—	—	—	—	—	—	—	15	—	—
	Copolymer (10)	—	65	—	—	—	—	—	—	—	—	—
	Copolymer (11)	—	—	65	—	—	—	—	—	—	—	—
	Copolymer (12)	—	—	—	65	—	—	—	—	—	—	—
	Copolymer (13)	—	—	—	—	—	—	—	—	—	—	—
	Copolymer (14)	—	—	—	—	65	—	—	—	—	—	—
	Copolymer (15)	—	—	—	—	—	65	—	—	—	—	—
	Copolymer (16)	—	—	—	—	—	—	65	—	—	—	—
	Copolymer (17)	—	—	—	—	—	—	—	65	—	—	—
	Copolymer (18)	—	—	—	—	—	—	—	—	—	—	—
	Copolymer (19)	—	—	—	—	—	—	—	—	—	15	—
	Copolymer (20)	—	—	—	—	—	—	—	—	—	—	15
	Copolymer (21)	—	—	—	—	—	—	—	—	—	—	—
	Natural rubber	20	20	20	20	20	20	20	20	20	20	20
	Polybutadiene rubber	15	15	15	15	15	15	15	15	—	—	—
	Silica 2 (N2SA:	75	75	75	75	75	75	75	75	75	75	75
	110 m2/g)
	Silane coupling agent A	6	6	6	6	6	6	6	6	6	6	6
	Carbon black	5	5	5	5	5	5	5	5	5	5	5
	Oil	20	20	20	20	20	20	20	20	20	20	20
	Antioxidant	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5
	Stearic acid	2	2	2	2	2	2	2	2	2	2	2
	Zinc oxide	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5
	Wax	1	1	1	1	1	1	1	1	1	1	1
	Sulfur	2	2	2	2	2	2	2	2	2	2	2
	Vulcanization	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8
	accelerator 1
	Vulcanization	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2
	accelerator 2
Evaluation	Mixing and kneading	100	100	97	96	95	93	92	92	96	98	102
	processability index
	Low-heat-build-up	100	95	98	92	99	98	97	101	104	107	98
	property index
	tan δ peak temperature	−15	−15	−15	−15	−15	−15	−15	−15	−15	−15	−15
	Rubber strength index	100	105	103	108	103	102	104	102	99	97	99
	Abrasion resistance	100	101	99	97	93	92	96	88	101	102	95
	index
	Wet-grip performance	100	101	101	96	96	97	96	100	105	104	102
	index
	Handling stability	6	6	6	6	66	6	6	6	5.5	5.5	5.5

TABLE 7
Examples in which a compound represented by the formula (IV) is used as a Terminal modifier
		Example	Comparative Example	Example
		11	12	13	14	15	16	17	1	4	5	6	10	12	18	19	20
Formulation	Copolymer (8)	—	—	—	—	—	—	—	65	—	—	—	65	—	65	65	65
(parts by	Copolymer (12)	—	—	—	—	—	—	—	—	65	—	—	—	—	—	—	—
mass)	Copolymer (14)	—	—	—	—	—	—	—	—	—	65	—	—	—	—	—	—
	Copolymer (15)	—	—	—	—	—	—	—	—	—	—	65	—	—	—	—	—
	Copolymer (19)	—	—	—	—	—	—	—	—	—	—	—	15	—	—	—	—
	Copolymer (22)	65	—	—	—	—	—	—	—	—	—	—	—	—	—	—	—
	Copolymer (23)	—	65	—	—	—	—	—	—	—	—	—	—	—	—	—	—
	Copolymer (24)	—	—	65	—	—	—	—	—	—	—	—	—	—	—	—	—
	Copolymer (25)	—	—	—	65	—	—	—	—	—	—	—	—	—	—	—	—
	Copolymer (26)	—	—	—	—	65	—	—	—	—	—	—	—	—	—	—	—
	Copolymer (27)	—	—	—	—	—	—	—	—	—	—	—	—	—	15	—	—
	Copolymer (28)	—	—	—	—	—	65	—	—	—	—	—	—	—	—	—	—
	Copolymer (29)	—	—	—	—	—	—	65	—	—	—	—	—	—	—	—	—
	Copolymer (30)	—	—	—	—	—	—	—	—	—	—	—	—	65	—	—	—
	Copolymer (31)	—	—	—	—	—	—	—	—	—	—	—	—	—	—	15	—
	Copolymer (32)	—	—	—	—	—	—	—	—	—	—	—	—	—	—	—	15
	Natural rubber	20	20	20	20	20	20	20	20	20	20	20	20	20	20	20	20
	Polybutadiene	15	15	15	15	15	15	15	15	15	15	15	—	15	—	—	—
	rubber
	Silica 2 (N2SA:	75	75	75	75	75	75	75	75	75	75	75	75	75	75	75	75
	110 m2/g)
	Silane coupling	6	6	6	6	6	6	6	6	6	6	6	6	6	6	6	6
	agent A
	Carbon black	5	5	5	5	5	5	5	5	5	5	5	5	5	5	5	5
	Oil	20	20	20	20	20	20	20	20	20	20	20	20	20	20	20	20
	Antioxidant	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5
	Stearic acid	2	2	2	2	2	2	2	2	2	2	2	2	2	2	2	2
	Zinc oxide	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5
	Wax	1	1	1	1	1	1	1	1	1	1	1	1	1	1	1	1
	Sulfur	2	2	2	2	2	2	2	2	2	2	2	2	2	2	2	2
	Vulcanization	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8
	accelerator 1
	Vulcanization	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2
	accelerator 2
Evaluation	Mixing and kneading	100	101	104	100	106	107	103	100	96	95	93	98	98	100	102	100
	processability index
	Low-heat-build-up	135	130	129	128	125	123	113	100	92	99	98	107	95	103	110	105
	property index
	tan δ peak	−15	−15	−15	−15	−15	−15	−15	−15	−15	−15	−15	−15	−15	−15	−15	−15
	temperature
	Rubber strength	105	104	104	105	106	103	107	100	108	103	102	97	103	101	103	102
	index
	Abrasion resistance	111	108	112	111	109	110	112	100	97	93	92	102	98	108	110	112
	index
	Wet-grip	110	109	108	106	112	109	107	100	96	96	97	104	97	104	108	106
	performance index
	Handling stability	6	6	6	6	6	6	6	6	6	6	6	5.5	6	6	6	6

TABLE 8
Examples in which a compound represented by the formula (IIId) is used as a Terminal modifier
				Com.
		Com. Ex.	Ex.	Ex.
		1	4	6	21	22	23	24	25	26	27	13
Formulation	Copolymer (7)	—	—	65	65	65	65	65	65	65	65	65
(parts by mass)	Copolymer (8)	65	—	—	—	—	—	—	—	—	—	—
	Copolymer (12)	—	65	—	—	—	—	—	—	—	—	—
	Natural rubber	20	20	20	20	20	20	20	20	20	20	20
	Polybutadiene rubber	15	15	15	15	15	15	15	15	15	15	15
	Silica 1 (N2SA: 80 m2/g)	—	—	—	—	—	—	—	—	—	—	—
	Silica 2 (N2SA: 110 m2/g)	75	75	75	75	75	75	75	60	15	37.5	6
	Silica 3 (N2SA: 160 m2/g)	—	—	—	—	—	—	—	15	60	37.5	3
	Silica 4 (N2SA: 200 m2/g)	—	—	—	—	—	—	—	—	—	—	—
	Silane coupling agent A	6	6	6	—	—	1.5	1.5	—	—	—	—
	Silane coupling agent B	—	—	—	6	—	6	—	—	—	—	—
	Silane coupling agent C	—	—	—	—	3.75	—	3.75	3.75	3.75	3.75	3.75
	Carbon black	5	5	5	5	5	5	5	5	5	5	5
	Coumarone indene resin 1	—	—	—	—	—	—	—	—	—	—	—
	(Tg: 90° C.)
	Coumarone indene resin 2	—	—	—	—	—	—	—	—	—	—	—
	(Tg: 10° C.)
	Coumarone indene resin 3	—	—	—	—	—	—	—	—	—	—	—
	(Tg: −30° C.)
	α-Methyl styrene resin	—	—	—	—	—	—	—	—	—	—	—
	(Tg: 95° C.)
	Oil	20	20	20	20	20	20	20	20	20	20	20
	Antioxidant	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5
	Stearic acid	2	2	2	2	2	2	2	2	2	2	2
	Zinc oxide	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5
	Wax	1	1	1	1	1	1	1	1	1	1	1
	Sulfur	2	2	2	2	2	2	2	2	2	2	2
	Vulcanization accelerator 1	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8
	Vulcanization accelerator 2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2
Evaluation	Mixing and kneading	100	96	101	102	106	105	110	105	100	103	125
	processability index
	Low-heat-build-up	100	92	143	145	148	145	148	146	135	140	160
	property index
	tan δ peak temperature	−15	−15	−15	−15	−15	−15	−15	−15	−15	−15	−15
	Rubber strength index	100	108	100	101	105	103	106	108	115	110	80
	Abrasion resistance index	100	97	104	100	102	102	105	105	110	108	75
	Wet-grip performance index	100	96	114	115	115	115	115	116	118	117	75
	Handling stability	6	6	6.25	6.25	6.25	6.25	6.5	6.25	6.5	6.5	4
		Com.		Com.
		Ex.	Ex.	Ex.
		14	28	29	30	31	32	33	34	35	36	15
Formulation	Copolymer (7)	65	65	65	65	65	65	65	65	65	55	100
(parts by mass)	Copolymer (8)	—	—	—	—	—	—	—	—	—	—	—
	Copolymer (12)	—	—	—	—	—	—	—	—	—	—	—
	Natural rubber	20	20	20	20	20	20	20	20	20	30	—
	Polybutadiene rubber	15	15	15	15	15	15	15	15	15	15	—
	Silica 1 (N2SA: 80 m2/g)	—	60	60	—	—	—	—	—	—	—	—
	Silica 2 (N2SA: 110 m2/g)	120	—	—	60	75	75	75	75	60	75	75
	Silica 3 (N2SA: 160 m2/g)	40	15	—	—	—	—	—	—	15	—	—
	Silica 4 (N2SA: 200 m2/g)	—	—	15	15	—	—	—	—	—	—	—
	Silane coupling agent A	—	—	—	—	—	—	—	—	—	6	6
	Silane coupling agent B	—	—	—	—	—	—	—	—	—	—	—
	Silane coupling agent C	3.75	3.75	3.75	3.75	3.75	3.75	3.75	3.75	3.75	—	—
	Carbon black	5	5	5	5	5	5	5	5	5	5	5
	Coumarone indene resin 1	—	—	—	—	10	—	10	10	10	—	—
	(Tg: 90° C.)
	Coumarone indene resin 2	—	—	—	—	—	—	5	—	—	—	—
	(Tg: 10° C.)
	Coumarone indene resin 3	—	—	—	—	—	—	—	5	—	—	—
	(Tg: −30° C.)
	α-Methyl styrene resin	—	—	—	—	—	10	—	—	—	—	—
	(Tg: 95° C.)
	Oil	20	20	20	20	10	10	5	5	10	20	20
	Antioxidant	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5
	Stearic acid	2	2	2	2	2	2	2	2	2	2	2
	Zinc oxide	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5
	Wax	1	1	1	1	1	1	1	1	1	1	1
	Sulfur	2	2	2	2	2	2	2	2	2	2	2
	Vulcanization accelerator 1	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8
	Vulcanization accelerator 2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2
Evaluation	Mixing and kneading	80	115	110	100	104	105	104	103	105	106	90
	processability index
	Low-heat-build-up	75	152	150	145	138	145	137	140	146	132	100
	property index
	tan δ peak temperature	−15	−15	−15	−7	−8	−7	−12	−15	−15	−15	−15
	Rubber strength index	90	102	104	108	106	105	106	107	108	115	95
	Abrasion resistance index	85	100	103	106	100	101	100	100	105	106	90
	Wet-grip performance index	128	115	116	117	120	125	122	124	116	102	120
	Handling stability	6.5	6	6.25	6.25	6.5	6.25	6.5	6.5	6.25	6.25	6.5

TABLE 9
Examples in which a compound represented by the formula (IIId) is used as a Terminal modifier
		Example
		37	38	39	40	41	21	42	43	44	45
Formulation	Copolymer (1)	65	—	—	—	—	—	—	—	—	—
(parts by mass)	Copolymer (2)	—	65	—	—	—	—	—	—	—	—
	Copolymer (3)	—	—	65	—	—	—	—	—	—	—
	Copolymer (4)	—	—	—	65	—	—	—	—	—	—
	Copolymer (5)	—	—	—	—	65	—	—	—	—	—
	Copolymer (6)	—	—	—	—	—	—	—	15	—	—
	Copolymer (7)	—	—	—	—	—	65	—	—	—	—
	Copolymer (8)	—	—	—	—	—	—	—	65	65	65
	Copolymer (9)	—	—	—	—	—	—	—	—	—	—
	Copolymer (10)	—	—	—	—	—	—	—	—	—	—
	Copolymer (11)	—	—	—	—	—	—	—	—	—	—
	Copolymer (12)	—	—	—	—	—	—	—	—	—	—
	Copolymer (13)	—	—	—	—	—	—	65	—	—	—
	Copolymer (14)	—	—	—	—	—	—	—	—	—	—
	Copolymer (15)	—	—	—	—	—	—	—	—	—	—
	Copolymer (16)	—	—	—	—	—	—	—	—	—	—
	Copolymer (17)	—	—	—	—	—	—	—	—	—	—
	Copolymer (18)	—	—	—	—	—	—	—	—	15	—
	Copolymer (19)	—	—	—	—	—	—	—	—	—	—
	Copolymer (20)	—	—	—	—	—	—	—	—	—	—
	Copolymer (21)	—	—	—	—	—	—	—	—	—	15
	Natural rubber	20	20	20	20	20	20	20	20	20	20
	Polybutadiene rubber	15	15	15	15	15	15	15	—	—	—
	Silica 2 (N2SA: 110 m2/g)	75	75	75	75	75	75	75	75	75	75
	Silane coupling agent B	6	6	6	6	6	6	6	6	6	6
	Silane coupling agent C	—	—	—	—	—	—	—	—	—	—
	Carbon black	5	5	5	5	5	5	5	5	5	5
	Oil	20	20	20	20	20	20	20	20	20	20
	Antioxidant	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5
	Stearic acid	2	2	2	2	2	2	2	2	2	2
	Zinc oxide	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5
	Wax	1	1	1	1	1	1	1	1	1	1
	Sulfur	2	2	2	2	2	2	2	2	2	2
	Vulcanization accelerator 1	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8
	Vulcanization accelerator 2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2
Evaluation	Mixing and kneading	105	106	103	111	101	102	106	101	101	104
	processability index
	Low-heat-build-up property	132	134	133	146	143	145	115	132	137	117
	index
	tan δ peak temperature	−15	−15	−15	−15	−15	−15	−15	−15	−15	−15
	Rubber strength index	103	104	105	102	101	101	104	101	101	102
	Abrasion resistance index	99	100	99	97	98	100	99	98	100	96
	Wet-grip performance index	110	110	109	110	108	115	115	115	115	115
	Handling stability	6.25	6.25	6.25	6.25	6.25	6.25	6.25	6	6	6
		Example
		46	47	48	49	50	22	51	52	53	54
Formulation	Copolymer (1)	65	—	—	—	—	—	—	—	—	—
(parts by mass)	Copolymer (2)	—	65	—	—	—	—	—	—	—	—
	Copolymer (3)	—	—	65	—	—	—	—	—	—	—
	Copolymer (4)	—	—	—	65	—	—	—	—	—	—
	Copolymer (5)	—	—	—	—	65	—	—	—	—	—
	Copolymer (6)	—	—	—	—	—	—	15	—	—	—
	Copolymer (7)	—	—	—	—	—	65	—	—	—	—
	Copolymer (8)	—	—	—	—	—	—	—	65	65	65
	Copolymer (9)	—	—	—	—	—	—	—	—	—	—
	Copolymer (10)	—	—	—	—	—	—	—	—	—	—
	Copolymer (11)	—	—	—	—	—	—	—	—	—	—
	Copolymer (12)	—	—	—	—	—	—	—	—	—	—
	Copolymer (13)	—	—	—	—	—	—	65	—	—	—
	Copolymer (14)	—	—	—	—	—	—	—	—	—	—
	Copolymer (15)	—	—	—	—	—	—	—	—	—	—
	Copolymer (16)	—	—	—	—	—	—	—	—	—	—
	Copolymer (17)	—	—	—	—	—	—	—	—	—	—
	Copolymer (18)	—	—	—	—	—	—	—	—	15	—
	Copolymer (19)	—	—	—	—	—	—	—	—	—	—
	Copolymer (20)	—	—	—	—	—	—	—	—	—	—
	Copolymer (21)	—	—	—	—	—	—	—	—	—	15
	Natural rubber	20	20	20	20	20	20	20	20	20	20
	Polybutadiene rubber	15	15	15	15	15	15	15	—	—	—
	Silica 2 (N2SA: 110 m2/g)	75	75	75	75	75	75	75	75	75	75
	Silane coupling agent B	—	—	—	—	—	—	—	—	—	—
	Silane coupling agent C	3.75	3.75	3.75	3.75	3.75	3.75	3.75	3.75	3.75	3.75
	Carbon black	5	5	5	5	5	5	5	5	5	5
	Oil	20	20	20	20	20	20	20	20	20	20
	Antioxidant	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5
	Stearic acid	2	2	2	2	2	2	2	2	2	2
	Zinc oxide	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5
	Wax	1	1	1	1	1	1	1	1	1	1
	Sulfur	2	2	2	2	2	2	2	2	2	2
	Vulcanization accelerator 1	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8
	Vulcanization accelerator 2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2
Evaluation	Mixing and kneading	109	110	107	115	105	106	110	105	105	108
	processability index
	Low-heat-build-up property	135	137	136	149	146	148	118	135	140	120
	index
	tan δ peak temperature	−15	−15	−15	−15	−15	−15	−15	−15	−15	−15
	Rubber strength index	107	108	109	106	105	105	108	105	105	106
	Abrasion resistance index	101	102	101	99	100	102	101	100	102	98
	Wet-grip performance index	114	114	113	112	112	115	110	109	110	108
	Handling stability	6.25	6.25	6.25	6.25	6.25	6.25	6	6	6	6

TABLE 10
Examples in which a compound represented by the formula (IV) is used as a Terminal modifier
		Example
		55	56	57	58	59	60	61	62	63	64
Formulation	Copolymer (8)	—	—	—	—	—	—	—	65	65	65
(parts by mass)	Copolymer (22)	65	—	—	—	—	—	—	—	—	—
	Copolymer (23)	—	65	—	—	—	—	—	—	—	—
	Copolymer (24)	—	—	65	—	—	—	—	—	—	—
	Copolymer (25)	—	—	—	65	—	—	—	—	—	—
	Copolymer (26)	—	—	—	—	65	—	—	—	—	—
	Copolymer (27)	—	—	—	—	—	—	—	15	—	—
	Copolymer (28)	—	—	—	—	—	65	—	—	—	—
	Copolymer (29)	—	—	—	—	—	—	65	—	—	—
	Copolymer (30)	—	—	—	—	—	—	—	—	—	—
	Copolymer (31)	—	—	—	—	—	—	—	—	15	—
	Copolymer (32)	—	—	—	—	—	—	—	—	—	15
	Natural rubber	20	20	20	20	20	20	20	20	20	20
	Polybutadiene rubber	15	15	15	15	15	15	15	—	—	—
	Silica 2 (N2SA: 110 m2/g)	75	75	75	75	75	75	75	75	75	75
	Silane coupling agent B	6	6	6	6	6	6	6	6	6	6
	Silane coupling agent C	—	—	—	—	—	—	—	—	—	—
	Carbon black	5	5	5	5	5	5	5	5	5	5
	Oil	20	20	20	20	20	20	20	20	20	20
	Antioxidant	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5
	Stearic acid	2	2	2	2	2	2	2	2	2	2
	Zinc oxide	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5
	Wax	1	1	1	1	1	1	1	1	1	1
	Sulfur	2	2	2	2	2	2	2	2	2	2
	Vulcanization accelerator 1	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8
	Vulcanization accelerator 2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2
Evaluation	Mixing and kneading	98	99	102	98	104	105	101	98	100	98
	processability index
	Low-heat-build-up property	143	138	137	136	133	131	121	111	118	113
	index
	tan δ peak temperature	−20	−20	−20	−20	−20	−20	−20	−20	−20	−20
	Rubber strength index	105	104	104	105	106	103	107	101	103	102
	Abrasion resistance index	107	104	108	107	105	106	108	104	106	108
	Wet-grip performance index	113	112	111	109	115	112	110	107	111	109
	Handling stability	6	6	6	6	6	6	6	6	6	6
		Example
		65	66	67	68	69	70	71	72	73	74
Formulation	Copolymer (8)	—	—	—	—	—	—	—	65	65	65
(parts by mass)	Copolymer (22)	65	—	—	—	—	—	—	—	—	—
	Copolymer (23)	—	65	—	—	—	—	—	—	—	—
	Copolymer (24)	—	—	65	—	—	—	—	—	—	—
	Copolymer (25)	—	—	—	65	—	—	—	—	—	—
	Copolymer (26)	—	—	—	—	65	—	—	—	—	—
	Copolymer (27)	—	—	—	—	—	—	—	15	—	—
	Copolymer (28)	—	—	—	—	—	65	—	—	—	—
	Copolymer (29)	—	—	—	—	—	—	65	—	—	—
	Copolymer (30)	—	—	—	—	—	—	—	—	—	—
	Copolymer (31)	—	—	—	—	—	—	—	—	15	—
	Copolymer (32)	—	—	—	—	—	—	—	—	—	15
	Natural rubber	20	20	20	20	20	20	20	20	20	20
	Polybutadiene rubber	15	15	15	15	15	15	15	—	—	—
	Silica 2 (N2SA: 110 m2/g)	75	75	75	75	75	75	75	75	75	75
	Silane coupling agent B	—	—	—	—	—	—	—	—	—	—
	Silane coupling agent C	3.75	3.75	3.75	3.75	3.75	3.75	3.75	3.75	3.75	3.75
	Carbon black	5	5	5	5	5	5	5	5	5	5
	Oil	20	20	20	20	20	20	20	20	20	20
	Antioxidant	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5
	Stearic acid	2	2	2	2	2	2	2	2	2	2
	Zinc oxide	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5
	Wax	1	1	1	1	1	1	1	1	1	1
	Sulfur	2	2	2	2	2	2	2	2	2	2
	Vulcanization accelerator 1	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8
	Vulcanization accelerator 2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2
Evaluation	Mixing and kneading	104	105	108	104	110	111	107	104	106	104
	processability index
	Low-heat-build-up property	143	138	137	136	133	131	121	111	118	113
	index
	tan δ peak temperature	−20	−20	−20	−20	−20	−20	−20	−20	−20	−20
	Rubber strength index	109	108	108	109	110	107	111	105	107	106
	Abrasion resistance index	109	106	110	109	107	108	110	106	108	110
	Wet-grip performance index	113	112	111	109	115	112	110	107	111	109
	Handling stability	6	6	6	6	6	6	6	6	6	6

TABLE 11
Examples in which a compound represented by the formula (IIIb) is used as a Terminal modifier
	Example
		75	76	77	78	79	80	81	82	83	84	85
Formulation	Copolymer (33)	65	—	—	—	—	—	—	—	—	65	—
(parts by	Copolymer (34)	—	65	—	—	—	—	—	—	—	—	65
mass)	Copolymer (35)	—	—	65	—	—	—	—	—	—	—	—
	Copolymer (36)	—	—	—	65	—	—	—	—	—	—	—
	Copolymer (37)	—	—	—	—	65	—	—	—	—	—	—
	Copolymer (38)	—	—	—	—	—	65	—	—	—	—	—
	Copolymer (39)	—	—	—	—	—	—	65	—	—	—	—
	Copolymer (40)	—	—	—	—	—	—	—	65	—	—	—
	Copolymer (41)	—	—	—	—	—	—	—	—	65	—	—
	Copolymer (42)	—	—	—	—	—	—	—	—	—	—	—
	Natural rubber	20	20	20	20	20	20	20	20	20	20	20
	Polybutadiene rubber	15	15	15	15	15	15	15	15	15	15	15
	Silica 2 (N2SA: 110 m2/g)	75	75	75	75	75	75	75	75	75	75	75
	Silane coupling agent B	6	6	6	6	6	6	6	6	6	—	—
	Silane coupling agent C	—	—	—	—	—	—	—	—	—	3.75	3.75
	Carbon black	5	5	5	5	5	5	5	5	5	5	5
	Oil	20	20	20	20	20	20	20	20	20	20	20
	Antioxidant	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5
	Stearic acid	2	2	2	2	2	2	2	2	2	2	2
	Zinc oxide	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5
	Wax	1	1	1	1	1	1	1	1	1	1	1
	Sulfur	2	2	2	2	2	2	2	2	2	2	2
	Vulcanization accelerator 1	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8
	Vulcanization accelerator 2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2
Evaluation	Mixing and kneading process-	102	107	103	102	103	107	102	103	101	107	112
	ability index
	Low-heat-build-property index	123	119	120	113	123	110	120	106	104	127	123
	tan δ peak temperature	−15	−15	−15	−15	−15	−15	−15	−15	−15	−15	−15
	Rubber strength index	103	104	103	105	102	105	103	107	105	108	109
	Abrasion resistance index	102	102	101	104	102	103	101	104	103	100	100
	Wet-grip performance index	104	104	103	113	103	112	106	109	108	105	105
	Handling stability	6	6	6	6	6	6	6	6	6	6	6
	Example	Com. Ex.
		86	87	88	89	90	91	92	16	17
Formulation	Copolymer (33)	—	—	—	—	—	—	—	—	—
(parts by	Copolymer (34)	—	—	—	—	—	—	—	—	—
mass)	Copolymer (35)	65	—	—	—	—	—	—	—	—
	Copolymer (36)	—	65	—	—	—	—	—	—	—
	Copolymer (37)	—	—	65	—	—	—	—	—	—
	Copolymer (38)	—	—	—	65	—	—	—	—	—
	Copolymer (39)	—	—	—	—	65	—	—	—	—
	Copolymer (40)	—	—	—	—	—	65	—	—	—
	Copolymer (41)	—	—	—	—	—	—	65	—	—
	Copolymer (42)	—	—	—	—	—	—	—	65	65
	Natural rubber	20	20	20	20	20	20	20	20	20
	Polybutadiene rubber	15	15	15	15	15	15	15	15	15
	Silica 2 (N2SA: 110 m2/g)	75	75	75	75	75	75	75	75	75
	Silane coupling agent B	—	—	—	—	—	—	—	6	—
	Silane coupling agent C	3.75	3.75	3.75	3.75	3.75	3.75	3.75	—	3.75
	Carbon black	5	5	5	5	5	5	5	5	5
	Oil	20	20	20	20	20	20	20	20	20
	Antioxidant	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5
	Stearic acid	2	2	2	2	2	2	2	2	2
	Zinc oxide	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5
	Wax	1	1	1	1	1	1	1	1	1
	Sulfur	2	2	2	2	2	2	2	2	2
	Vulcanization accelerator 1	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8
	Vulcanization accelerator 2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2
Evaluation	Mixing and kneading process-	108	107	108	112	107	108	106	90	94
	ability index
	Low-heat-build-property index	124	117	127	114	124	110	108	95	98
	tan δ peak temperature	−15	−15	−15	−15	−15	−15	−15	−15	−15
	Rubber strength index	108	110	107	110	108	112	110	97	102
	Abrasion resistance index	99	102	100	101	99	102	101	95	93
	Wet-grip performance index	104	114	104	113	107	110	109	102	103
	Handling stability	6	6	6	6	6	6	6	6	6

TABLE 12
Examples in which a compound containing an alkoxysilyl group, a
nitrogen atom and a carbonyl group is used as a Terminal modifier
	Example
		93	94	95	96	97	98	99	100
Formulation	Copolymer (43)	65	—	—	—	—	—	65	—
(parts by	Copolymer (44)	—	65	—	—	—	—	—	65
mass)	Copolymer (45)	—	—	65	—	—	—	—	—
	Copolymer (46)	—	—	—	65	—	—	—	—
	Copolymer (47)	—	—	—	—	65	—	—	—
	Copolymer (48)	—	—	—	—	—	65	—	—
	Copolymer (49)	—	—	—	—	—	—	—	—
	Natural rubber	20	20	20	20	20	20	20	20
	Polybutadiene rubber	15	15	15	15	15	15	15	15
	Silica 2 (N2SA: 110 m2/g)	75	75	75	75	75	75	75	75
	Silane coupling agent B	6	6	6	6	6	6	—	—
	Silane coupling agent C	—	—	—	—	—	—	3.75	3.75
	Carbon black	5	5	5	5	5	5	5	5
	Oil	20	20	20	20	20	20	20	20
	Antioxidant	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5
	Stearic acid	2	2	2	2	2	2	2	2
	Zinc oxide	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5
	Wax	1	1	1	1	1	1	1	1
	Sulfur	2	2	2	2	2	2	2	2
	Vulcanization accelerator 1	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8
	Vulcanization accelerator 2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2
Evaluation	Mixing and kneading processability index	106	105	103	102	100	105	111	110
	Low-heat-build-property index	118	110	117	114	118	109	122	114
	tan δ peak temperature	−15	−15	−15	−15	−15	−15	−15	−15
	Rubber strength index	100	102	100	101	100	103	105	107
	Abrasion resistance index	107	106	102	103	104	103	105	104
	Wet-grip performance index	103	109	107	110	111	111	104	110
	Handling stability	6	6	6	6	6	6	6	6
	Example	Com. Ex.
			101	102	103	104	18	19
	Formulation	Copolymer (43)	—	—	—	—	—	—
	(parts by	Copolymer (44)	—	—	—	—	—	—
	mass)	Copolymer (45)	65	—	—	—	—	—
		Copolymer (46)	—	65	—	—	—	—
		Copolymer (47)	—	—	65	—	—	—
		Copolymer (48)	—	—	—	65	—	—
		Copolymer (49)	—	—	—	—	65	65
		Natural rubber	20	20	20	20	20	20
		Polybutadiene rubber	15	15	15	15	15	15
		Silica 2 (N2SA: 110 m2/g)	75	75	75	75	75	75
		Silane coupling agent B	—	—	—	—	6	—
		Silane coupling agent C	3.75	3.75	3.75	3.75	—	3.75
		Carbon black	5	5	5	5	5	5
		Oil	20	20	20	20	20	20
		Antioxidant	1.5	1.5	1.5	1.5	1.5	1.5
		Stearic acid	2	2	2	2	2	2
		Zinc oxide	2.5	2.5	2.5	2.5	2.5	2.5
		Wax	1	1	1	1	1	1
		Sulfur	2	2	2	2	2	2
		Vulcanization accelerator 1	1.8	1.8	1.8	1.8	1.8	1.8
		Vulcanization accelerator 2	1.2	1.2	1.2	1.2	1.2	1.2
	Evaluation	Mixing and kneading processability index	108	107	105	110	92	97
		Low-heat-build-property index	121	118	122	113	92	95
		tan δ peak temperature	−15	−15	−15	−15	−15	−15
		Rubber strength index	105	106	105	108	96	101
		Abrasion resistance index	100	101	102	101	94	92
		Wet-grip performance index	108	111	112	112	100	101
		Handling stability	6	6	6	6	6	6

TABLE 13
Examples in which an N,N-dialkyl-substituted carboxylic acid
amide dialkyl acetal compound is used as a Terminal modifier
	Example
		105	106	107	108	109	110	111	112
Formulation	Copolymer (50)	65	—	—	—	—	—	65	—
(parts by	Copolymer (51)	—	65	—	—	—	—	—	65
mass)	Copolymer (52)	—	—	65	—	—	—	—	—
	Copolymer (53)	—	—	—	65	—	—	—	—
	Copolymer (54)	—	—	—	—	65	—	—	—
	Copolymer (55)	—	—	—	—	—	65	—	—
	Copolymer (56)	—	—	—	—	—	—	—	—
	Natural rubber	20	20	20	20	20	20	20	20
	Polybutadiene rubber	15	15	15	15	15	15	15	15
	Silica 2 (N2SA: 110 m2/g)	75	75	75	75	75	75	75	75
	Silane coupling agent B	6	6	6	6	6	6	—	—
	Silane coupling agent C	—	—	—	—	—	—	3.75	3.75
	Carbon black	5	5	5	5	5	5	5	5
	Oil	20	20	20	20	20	20	20	20
	Antioxidant	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5
	Stearic acid	2	2	2	2	2	2	2	2
	Zinc oxide	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5
	Wax	1	1	1	1	1	1	1	1
	Sulfur	2	2	2	2	2	2	2	2
	Vulcanization accelerator 1	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8
	Vulcanization accelerator 2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2
Evaluation	Mixing and kneading processability index	103	105	104	104	100	106	108	110
	Low-heat-build-property index	119	112	110	116	115	107	123	116
	tan δ peak temperature	−15	−15	−15	−15	−15	−15	−15	−15
	Rubber strength index	101	102	100	100	101	103	106	107
	Abrasion resistance index	108	107	103	102	103	102	106	105
	Wet-grip performance index	102	107	111	108	113	110	103	108
	Handling stability	6	6	6	6	6	6	6	6
	Example	Com. Ex.
			113	114	115	116	20	21
	Formulation	Copolymer (50)	—	—	—	—	—	—
	(parts by	Copolymer (51)	—	—	—	—	—	—
	mass)	Copolymer (52)	65	—	—	—	—	—
		Copolymer (53)	—	65	—	—	—	—
		Copolymer (54)	—	—	65	—	—	—
		Copolymer (55)	—	—	—	65	—	—
		Copolymer (56)	—	—	—	—	65	65
		Natural rubber	20	20	20	20	20	20
		Polybutadiene rubber	15	15	15	15	15	15
		Silica 2 (N2SA: 110 m2/g)	75	75	75	75	75	75
		Silane coupling agent B	—	—	—	—	6	—
		Silane coupling agent C	3.75	3.75	3.75	3.75	—	3.75
		Carbon black	5	5	5	5	5	5
		Oil	20	20	20	20	20	20
		Antioxidant	1.5	1.5	1.5	1.5	1.5	1.5
		Stearic acid	2	2	2	2	2	2
		Zinc oxide	2.5	2.5	2.5	2.5	2.5	2.5
		Wax	1	1	1	1	1	1
		Sulfur	2	2	2	2	2	2
		Vulcanization accelerator 1	1.8	1.8	1.8	1.8	1.8	1.8
		Vulcanization accelerator 2	1.2	1.2	1.2	1.2	1.2	1.2
	Evaluation	Mixing and kneading processability index	109	109	105	111	90	94
		Low-heat-build-property index	114	120	119	111	92	95
		tan δ peak temperature	−15	−15	−15	−15	−15	−15
		Rubber strength index	105	105	106	108	96	101
		Abrasion resistance index	101	100	101	100	93	91
		Wet-grip performance index	112	109	114	111	100	101
		Handling stability	6	6	6	6	6	6

TABLE 14
Examples in which a compound represented by the formula (IIId) is used as a Terminal modifier
			Comparative
		Example	Example
		117	118	119	120	121	122	123	124	125	126	22	23
Formulation	Copolymer (1)	60	—	—	—	—	—	—	—	—	—	—	—
(parts by	Copolymer (2)	—	60	—	—	—	—	—	—	—	—	—	—
mass)	Copolymer (3)	—	—	60	—	—	—	—	—	—	—	—	—
	Copolymer (4)	—	—	—	60	—	—	—	—	—	—	—	—
	Copolymer (5)	—	—	—	—	60	—	—	—	—	—	—	—
	Copolymer (6)	—	—	—	—	—	—	—	20	—	—	—	—
	Copolymer (7)	—	—	—	—	—	60	—	—	—	—	—	—
	Copolymer (8)	—	—	—	—	—	—	—	60	60	60	60	—
	Copolymer (9)	—	—	—	—	—	—	—	—	—	—	—	—
	Copolymer (10)	—	—	—	—	—	—	—	—	—	—	—	60
	Copolymer (11)	—	—	—	—	—	—	—	—	—	—	—	—
	Copolymer (12)	—	—	—	—	—	—	—	—	—	—	—	—
	Copolymer (13)	—	—	—	—	—	—	60	—	—	—	—	—
	Copolymer (14)	—	—	—	—	—	—	—	—	—	—	—	—
	Copolymer (15)	—	—	—	—	—	—	—	—	—	—	—	—
	Copolymer (16)	—	—	—	—	—	—	—	—	—	—	—	—
	Copolymer (17)	—	—	—	—	—	—	—	—	—	—	—	—
	Copolymer (18)	—	—	—	—	—	—	—	—	20	—	—	—
	Copolymer (19)	—	—	—	—	—	—	—	—	—	—	—	—
	Copolymer (20)	—	—	—	—	—	—	—	—	—	—	—	—
	Copolymer (21)	—	—	—	—	—	—	—	—	—	20	—	—
	Natural rubber	20	20	20	20	20	20	20	20	20	20	20	20
	Polybutadiene rubber	20	20	20	20	20	20	20	—	—	—	20	20
	Carbon black	15	15	15	15	15	15	15	15	15	15	15	15
	Oil	25	25	25	25	25	25	25	25	25	25	25	25
	Silica 1 (N2SA: 80 m2/g)	—	—	—	—	—	—	—	—	—	—	—	—
	Silica 2 (N2SA: 110 m2/g)	60	60	60	60	60	60	60	60	60	60	60	60
	Silica 3 (N2SA: 160 m2/g)	15	15	15	15	15	15	15	15	15	15	15	15
	Silica 4 (N2SA: 200 m2/g)	—	—	—	—	—	—	—	—	—	—	—	—
	Silane coupling agent A	6	6	6	6	6	6	6	6	6	6	6	6
	Antioxidant	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5
	Stearic acid	2	2	2	2	2	2	2	2	2	2	2	2
	Zinc oxide	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5
	Wax	1	1	1	1	1	1	1	1	1	1	1	1
	Sulfur	2	2	2	2	2	2	2	2	2	2	2	2
	Carbon black	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8
	Oil	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2
Evaluation	Mixing and kneading process-	105	106	103	111	101	102	106	101	101	104	100	102
	ability index
	Low-heat-build-property	125	127	126	138	135	137	109	125	130	111	100	96
	index
	tan δ peak temperature	−14	−14	−14	−14	−14	−14	−13	−14	−13	−13	−14	−14
	Rubber strength index	107	108	109	106	105	105	108	105	104	106	100	106
	Abrasion resistance index	101	102	101	99	100	102	101	100	102	98	100	99
	Wet-grip performance index	114	114	113	112	112	115	110	109	110	108	100	103
	Handling stability	6.25	6.25	6.25	6.25	6.25	6.25	6.25	6	6	6	6	6
	Comparative Example
			24	25	26	27	28	29	30	31	32
	Formulation	Copolymer (1)	—	—	—	—	—	—	—	—	—
	(parts by	Copolymer (2)	—	—	—	—	—	—	—	—	—
	mass)	Copolymer (3)	—	—	—	—	—	—	—	—	—
		Copolymer (4)	—	—	—	—	—	—	—	—	—
		Copolymer (5)	—	—	—	—	—	—	—	—	—
		Copolymer (6)	—	—	—	—	—	—	—	—	—
		Copolymer (7)	—	—	—	—	—	—	—	—	—
		Copolymer (8)	—	—	—	—	—	—	60	60	60
		Copolymer (9)	—	—	—	—	—	—	20	—	—
		Copolymer (10)	—	—	—	—	—	—	—	—	—
		Copolymer (11)	60	—	—	—	—	—	—	—	—
		Copolymer (12)	—	60	—	—	—	—	—	—	—
		Copolymer (13)	—	—	—	—	—	—	—	—	—
		Copolymer (14)	—	—	60	—	—	—	—	—	—
		Copolymer (15)	—	—	—	60	—	—	—	—	—
		Copolymer (16)	—	—	—	—	60	—	—	—	—
		Copolymer (17)	—	—	—	—	—	60	—	—	—
		Copolymer (18)	—	—	—	—	—	—	—	—	—
		Copolymer (19)	—	—	—	—	—	—	—	20	—
		Copolymer (20)	—	—	—	—	—	—	—	—	20
		Copolymer (21)	—	—	—	—	—	—	—	—	—
		Natural rubber	20	20	20	20	20	20	20	20	20
		Polybutadiene rubber	20	20	20	20	20	20	—	—	—
		Carbon black	15	15	15	15	15	15	15	15	15
		Oil	25	25	25	25	25	25	25	25	25
		Silica 1 (N2SA; 80 m2/g)	—	—	—	—	—	—	—	—	—
		Silica 2 (N2SA: 110 m2/g)	60	60	60	60	60	60	60	60	60
		Silica 3 (N2SA: 160 m2/g)	15	15	15	15	15	15	15	15	15
		Silica 4 (N2SA: 200 m2/g)	—	—	—	—	—	—	—	—	—
		Silane coupling agent A	6	6	6	6	6	6	6	6	6
		Antioxidant	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5
		Stearic acid	2	2	2	2	2	2	2	2	2
		Zinc oxide	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5
		Wax	1	1	1	1	1	1	1	1	1
		Sulfur	2	2	2	2	2	2	2	2	2
		Carbon black	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8
		Oil	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2
	Evaluation	Mixing and kneading process-	98	97	96	94	93	93	97	98	102
		ability index
		Low-heat-build-property	99	93	100	99	98	102	105	107	98
		index
		tan δ peak temperature	−14	−16	−14	−14	−14	−14	−14	−13	−13
		Rubber strength index	104	109	104	103	105	103	100	100	102
		Abrasion resistance index	97	95	91	90	94	87	99	100	93
		Wet-grip performance index	103	98	98	99	98	102	107	106	104
		Handling stability	6	5.75	6	6	6	6	5.5	5.5	5.5

TABLE 15
Examples in which a compound represented by the formula (IV) is used as a Terminal modifier
			Comparative
		Example	Example
		127	128	129	130	131	132	133	22	25
Formulation	Copolymer (8)	—	—	—	—	—	—	—	60	—
(parts by	Copolymer (12)	—	—	—	—	—	—	—	—	60
mass)	Copolymer (14)	—	—	—	—	—	—	—	—	—
	Copolymer (15)	—	—	—	—	—	—	—	—	—
	Copolymer (19)	—	—	—	—	—	—	—	—	—
	Copolymer (22)	60	—	—	—	—	—	—	—	—
	Copolymer (23)	—	60	—	—	—	—	—	—	—
	Copolymer (24)	—	—	60	—	—	—	—	—	—
	Copolymer (25)	—	—	—	60	—	—	—	—	—
	Copolymer (26)	—	—	—	—	60	—	—	—	—
	Copolymer (27)	—	—	—	—	—	—	—	—	—
	Copolymer (28)	—	—	—	—	—	60	—	—	—
	Copolymer (29)	—	—	—	—	—	—	60	—	—
	Copolymer (30)	—	—	—	—	—	—	—	—	—
	Copolymer (31)	—	—	—	—	—	—	—	—	—
	Copolymer (32)	—	—	—	—	—	—	—	—	—
	Natural rubber	20	20	20	20	20	20	20	20	20
	Polybutadiene rubber	20	20	20	20	20	20	20	20	20
	Carbon black	15	15	15	15	15	15	15	15	15
	Oil	25	25	25	25	25	25	25	25	25
	Silica 1 (N2SA: 80 m2/g)	—	—	—	—	—	—	—	—	—
	Silica 2 (N2SA: 110 m2/g)	60	60	60	60	60	60	60	60	60
	Silica 3 (N2SA: 160 m2/g)	15	15	15	15	15	15	15	15	15
	Silica 4 (N2SA: 200 m2/g)	—	—	—	—	—	—	—	—	—
	Silane coupling agent A	6	6	6	6	6	6	6	6	6
	Antioxidant	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5
	Stearic acid	2	2	2	2	2	2	2	2	2
	Zinc oxide	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5
	Wax	1	1	1	1	1	1	1	1	1
	Sulfur	2	2	2	2	2	2	2	2	2
	Vulcanization accelerator 1	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8
	Vulcanization accelerator 2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2
Evaluation	Mixing and kneading processability index	100	101	104	100	106	107	103	100	97
	Low-heat-build-property index	129	126	127	126	122	123	113	100	93
	tan δ peak temperature	−14	−14	−14	−14	−14	−14	−14	−14	−16
	Rubber strength index	111	110	109	111	112	109	113	100	109
	Abrasion resistance index	109	106	110	109	107	108	110	100	95
	Wet-grip performance index	110	109	108	111	112	110	109	100	98
	Handling stability	6	6	6	6	6	6	6	6	5.75
	Comparative Example	Example
			26	27	31	33	134	135	136
	Formulation	Copolymer (8)	—	—	60	—	60	60	60
	(parts by	Copolymer (12)	—	—	—	—	—	—	—
	mass)	Copolymer (14)	60	—	—	—	—	—	—
		Copolymer (15)	—	60	—	—	—	—	—
		Copolymer (19)	—	—	20	—	—	—	—
		Copolymer (22)	—	—	—	—	—	—	—
		Copolymer (23)	—	—	—	—	—	—	—
		Copolymer (24)	—	—	—	—	—	—	—
		Copolymer (25)	—	—	—	—	—	—	—
		Copolymer (26)	—	—	—	—	—	—	—
		Copolymer (27)	—	—	—	—	20	—	—
		Copolymer (28)	—	—	—	—	—	—	—
		Copolymer (29)	—	—	—	—	—	—	—
		Copolymer (30)	—	—	—	60	—	—	—
		Copolymer (31)	—	—	—	—	—	20	—
		Copolymer (32)	—	—	—	—	—	—	20
		Natural rubber	20	20	20	20	20	20	20
		Polybutadiene rubber	20	20	—	20	—	—	—
		Carbon black	15	15	15	15	15	15	15
		Oil	25	25	25	25	25	25	25
		Silica 1 (N2SA: 80 m2/g)	—	—	—	—	—	—	—
		Silica 2 (N2SA: 110 m2/g)	60	60	60	60	60	60	60
		Silica 3 (N2SA: 160 m2/g)	15	15	15	15	15	15	15
		Silica 4 (N2SA: 200 m2/g)	—	—	—	—	—	—	—
		Silane coupling agent A	6	6	6	6	6	6	6
		Antioxidant	1.5	1.5	1.5	1.5	1.5	1.5	1.5
		Stearic acid	2	2	2	2	2	2	2
		Zinc oxide	2.5	2.5	2.5	2.5	2.5	2.5	2.5
		Wax	1	1	1	1	1	1	1
		Sulfur	2	2	2	2	2	2	2
		Vulcanization accelerator 1	1.8	1.8	1.8	1.8	1.8	1.8	1.8
		Vulcanization accelerator 2	1.2	1.2	1.2	1.2	1.2	1.2	1.2
	Evaluation	Mixing and kneading processability index	96	94	98	98	101	102	100
		Low-heat-build-property index	100	99	107	96	108	110	105
		tan δ peak temperature	−14	−14	−13	−13	−13	−14	−14
		Rubber strength index	104	103	100	105	109	109	108
		Abrasion resistance index	91	90	100	100	106	108	110
		Wet-grip performance index	98	99	106	104	111	110	108
		Handling stability	6	6	5.5	5.5	6	6	6

TABLE 16
Examples in which a compound represented by the formula (IIId) is used as a Terminal modifier
	Com. Ex.	Ex.	Com. Ex.	Ex.
		22	25	122	34	35	137	138	139	140
Formulation	Copolymer (7)	—	—	60	60	60	60	60	60	60
(parts by	Copolymer (8)	60	—	—	—	—	—	—	—	—
mass)	Copolymer (12)	—	60	—	—	—	—	—	—	—
	Natural rubber	20	20	20	20	20	20	20	20	20
	Polybutadiene rubber	20	20	20	20	20	20	20	20	20
	Carbon black	15	15	15	15	15	15	15	15	15
	Oil	25	25	25	25	25	25	25	25	25
	Silica 1 (N2SA: 80 m2/g)	—	—	—	—	—	—	—	60	60
	Silica 2 (N2SA: 110 m2/g)	60	60	60	6	120	35	15	—	—
	Silica 3 (N2SA: 160 m2/g)	15	15	15	3	40	35	60	15	—
	Silica 4 (N2SA: 200 m2/g)	—	—	—	—	—	—	—	—	15
	Silane coupling agent A	6	6	6	6	6	6	6	6	6
	Coumarone indene resin 1 (Tg: 90° C.)	—	—	—	—	—	—	—	—	—
	Coumarone indene resin 2 (Tg: 10° C.)	—	—	—	—	—	—	—	—	—
	Coumarone indene resin 3 (Tg: −30° C.)	—	—	—	—	—	—	—	—	—
	α-Methyl styrene resin (Tg: 95° C.)	—	—	—	—	—	—	—	—	—
	Antioxidant	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5
	Stearic acid	2	2	2	2	2	2	2	2	2
	Zinc oxide	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5
	Wax	1	1	1	1	1	1	1	1	1
	Sulfur	2	2	2	2	2	2	2	2	2
	Vulcanization accelerator 1	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8
	Vulcanization accelerator 2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2
Evaluation	Mixing and kneading processability index	100	97	102	121	86	101	100	105	102
	Low-heat-build-property index	100	93	137	99	121	133	130	137	137
	tan δ peak temperature	−14	−16	−14	−14	−14	−16	−14	−14	−15
	Rubber strength index	100	109	105	91	125	106	111	102	107
	Abrasion resistance index	100	95	102	97	83	104	107	100	103
	Wet-grip performance index	100	98	115	96	111	115	113	113	116
	Handling stability	6	5.75	6.25	6.25	6	6	6.25	6	6
	Ex.	Com. Ex.
			141	142	143	144	145	146	36
	Formulation	Copolymer (7)	60	70	60	60	60	60	100
	(parts by	Copolymer (8)	—	—	—	—	—	—	—
	mass)	Copolymer (12)	—	—	—	—	—	—	—
		Natural rubber	20	10	20	20	20	20	—
		Polybutadiene rubber	20	20	20	20	20	20	—
		Carbon black	15	15	15	15	15	15	15
		Oil	25	25	25	25	25	25	25
		Silica 1 (N2SA: 80 m2/g)	—	—	—	—	—	—	—
		Silica 2 (N2SA: 110 m2/g)	60	60	60	60	60	60	60
		Silica 3 (N2SA: 160 m2/g)	—	15	15	15	15	15	15
		Silica 4 (N2SA: 200 m2/g)	15	—	—	—	—	—	—
		Silane coupling agent A	6	6	6	6	6	6	6
		Coumarone indene resin 1 (Tg: 90° C.)	—	—	10	—	10	10	—
		Coumarone indene resin 2 (Tg: 10° C.)	—	—	—	—	5	—	—
		Coumarone indene resin 3 (Tg: −30° C.)	—	—	—	—	—	5	—
		α-Methyl styrene resin (Tg: 95° C.)	—	—	—	10	—	—	—
		Antioxidant	1.5	1.5	1.5	1.5	1.5	1.5	1.5
		Stearic acid	2	2	2	2	2	2	2
		Zinc oxide	2.5	2.5	2.5	2.5	2.5	2.5	2.5
		Wax	1	1	1	1	1	1	1
		Sulfur	2	2	2	2	2	2	2
		Vulcanization accelerator 1	1.8	1.8	1.8	1.8	1.8	1.8	1.8
		Vulcanization accelerator 2	1.2	1.2	1.2	1.2	1.2	1.2	1.2
	Evaluation	Mixing and kneading processability index	101	104	102	102	108	110	82
		Low-heat-build-property index	132	131	137	136	134	137	125
		tan δ peak temperature	−16	−13	−14	−14	−14	−13	−10
		Rubber strength index	110	105	107	107	111	112	78
		Abrasion resistance index	105	103	104	100	102	105	79
		Wet-grip performance index	117	109	119	121	119	121	124
		Handling stability	6	6.5	6.25	6.25	6.25	6.5	4.5

TABLE 17
Examples in which a compound represented by the formula (IIIb) is used as a Terminal modifier
	Example
		147	148	149	150	151	152	153	154	155
Formulation	Copolymer (8)	—	—	—	—	—	—	—	—	—
(parts by	Copolymer (12)	—	—	—	—	—	—	—	—	—
mass)	Copolymer (14)	—	—	—	—	—	—	—	—	—
	Copolymer (15)	—	—	—	—	—	—	—	—	—
	Copolymer (19)	—	—	—	—	—	—	—	—	—
	Copolymer (33)	60	—	—	—	—	—	—	—	—
	Copolymer (34)	—	60	—	—	—	—	—	—	—
	Copolymer (35)	—	—	60	—	—	—	—	—	—
	Copolymer (36)	—	—	—	60	—	—	—	—	—
	Copolymer (37)	—	—	—	—	60	—	—	—	—
	Copolymer (38)	—	—	—	—	—	60	—	—	—
	Copolymer (39)	—	—	—	—	—	—	60	—	—
	Copolymer (40)	—	—	—	—	—	—	—	60	—
	Copolymer (41)	—	—	—	—	—	—	—	—	60
	Copolymer (42)	—	—	—	—	—	—	—	—	—
	Natural rubber	20	20	20	20	20	20	20	20	20
	Polybutadiene rubber	20	20	20	20	20	20	20	20	20
	Carbon black	15	15	15	15	15	15	15	15	15
	Oil	25	25	25	25	25	25	25	25	25
	Silica 1 (N2SA: 80 m2/g)	—	—	—	—	—	—	—	—	—
	Silica 2 (N2SA: 110 m2/g)	60	60	60	60	60	60	60	60	60
	Silica 3 (N2SA: 160 m2/g)	15	15	15	15	15	15	15	15	15
	Silica 4 (N2SA: 200 m2/g)	—	—	—	—	—	—	—	—	—
	Silane coupling agent A	6	6	6	6	6	6	6	6	6
	Antioxidant	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5
	Stearic acid	2	2	2	2	2	2	2	2	2
	Zinc oxide	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5
	Wax	1	1	1	1	1	1	1	1	1
	Sulfur	2	2	2	2	2	2	2	2	2
	Vulcanization accelerator 1	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8
	Vulcanization accelerator 2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2
Evaluation	Mixing and kneading processability index	111	117	112	111	112	117	111	112	110
	Low-heat-build-property index	126	121	123	115	126	112	123	108	106
	tan δ peak temperature	−15	−15	−15	−15	−15	−15	−15	−15	−15
	Rubber strength index	104	105	104	106	103	106	104	108	106
	Abrasion resistance index	101	101	100	103	101	102	100	103	102
	Wet-grip performance index	104	104	103	113	103	112	106	109	108
	Handling stability	6.25	6	6	6	6.25	6.25	6	6	6
	Comparative Example
			22	25	26	27	31	37
	Formulation	Copolymer (8)	60	—	—	—	60	—
	(parts by	Copolymer (12)	—	60	—	—	—	—
	mass)	Copolymer (14)	—	—	60	—	—	—
		Copolymer (15)	—	—	—	60	—	—
		Copolymer (19)	—	—	—	—	20	—
		Copolymer (33)	—	—	—	—	—	—
		Copolymer (34)	—	—	—	—	—	—
		Copolymer (35)	—	—	—	—	—	—
		Copolymer (36)	—	—	—	—	—	—
		Copolymer (37)	—	—	—	—	—	—
		Copolymer (38)	—	—	—	—	—	—
		Copolymer (39)	—	—	—	—	—	—
		Copolymer (40)	—	—	—	—	—	—
		Copolymer (41)	—	—	—	—	—	—
		Copolymer (42)	—	—	—	—	—	60
		Natural rubber	20	20	20	20	20	20
		Polybutadiene rubber	20	20	20	20	—	20
		Carbon black	15	15	15	15	15	15
		Oil	25	25	25	25	25	25
		Silica 1 (N2SA: 80 m2/g)	—	—	—	—	—	—
		Silica 2 (N2SA: 110 m2/g)	60	60	60	60	60	60
		Silica 3 (N2SA: 160 m2/g)	15	15	15	15	15	15
		Silica 4 (N2SA: 200 m2/g)	—	—	—	—	—	—
		Silane coupling agent A	6	6	6	6	6	6
		Antioxidant	1.5	1.5	1.5	1.5	1.5	1.5
		Stearic acid	2	2	2	2	2	2
		Zinc oxide	2.5	2.5	2.5	2.5	2.5	2.5
		Wax	1	1	1	1	1	1
		Sulfur	2	2	2	2	2	2
		Vulcanization accelerator 1	1.8	1.8	1.8	1.8	1.8	1.8
		Vulcanization accelerator 2	1.2	1.2	1.2	1.2	1.2	1.2
	Evaluation	Mixing and kneading processability index	100	97	96	94	98	98
		Low-heat-build-property index	100	93	100	99	107	97
		tan δ peak temperature	−14	−16	−14	−14	−13	−15
		Rubber strength index	100	109	104	103	100	98
		Abrasion resistance index	100	95	91	90	100	94
		Wet-grip performance index	100	98	98	99	106	102
		Handling stability	6	5.75	6	6	5.5	6

TABLE 18
Examples in which a compound containing an alkoxysilyl group, a
nitrogen atom and a carbonyl group is used as a Terminal modifier
	Example	Comparative Example
	156	157	158	159	160	161	22	25	26	27	31	38
Formulation	Copolymer (8)	—	—	—	—	—	—	60	—	—	—	60	—
(parts by	Copolymer (12)	—	—	—	—	—	—	—	60	—	—	—	—
mass)	Copolymer (14)	—	—	—	—	—	—	—	—	60	—	—	—
	Copolymer (15)	—	—	—	—	—	—	—	—	—	60	—	—
	Copolymer (19)	—	—	—	—	—	—	—	—	—	—	20	—
	Copolymer (43)	60	—	—	—	—	—	—	—	—	—	—	—
	Copolymer (44)	—	60	—	—	—	—	—	—	—	—	—	—
	Copolymer (45)	—	—	60	—	—	—	—	—	—	—	—	—
	Copolymer (46)	—	—	—	60	—	—	—	—	—	—	—	—
	Copolymer (47)	—	—	—	—	60	—	—	—	—	—	—	—
	Copolymer (48)	—	—	—	—	—	60	—	—	—	—	—	—
	Copolymer (49)	—	—	—	—	—	—	—	—	—	—	—	60
	Natural rubber	20	20	20	20	20	20	20	20	20	20	20	20
	Polybutadiene rubber	20	20	20	20	20	20	20	20	20	20	—	20
	Carbon black	15	15	15	15	15	15	15	15	15	15	15	15
	Oil	25	25	25	25	25	25	25	25	25	25	25	25
	Silica 1 (N2SA: 80 m2/g)	—	—	—	—	—	—	—	—	—	—	—	—
	Silica 2 (N2SA: 110 m2/g)	60	60	60	60	60	60	60	60	60	60	60	60
	Silica 3 (N2SA: 160 m2/g)	15	15	15	15	15	15	15	15	15	15	15	15
	Silica 4 (N2SA: 200 m2/g)	—	—	—	—	—	—	—	—	—	—	—	—
	Silane coupling agent A	6	6	6	6	6	6	6	6	6	6	6	6
	Antioxidant	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5
	Stearic acid	2	2	2	2	2	2	2	2	2	2	2	2
	Zinc oxide	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5
	Wax	1	1	1	1	1	1	1	1	1	1	1	1
	Sulfur	2	2	2	2	2	2	2	2	2	2	2	2
	Vulcanization accelerator 1	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8
	Vulcanization accelerator 2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2
Evaluation	Mixing and kneading	115	114	112	111	109	114	100	97	96	94	98	100
	processability index
	Low-heat-build-property	120	112	119	116	120	111	100	93	100	99	107	94
	index
	tan δ peak temperature	−15	−15	−15	−15	−15	−15	−14	−16	−14	−14	−13	−15
	Rubber strength index	101	103	101	102	101	104	100	109	104	103	100	97
	Abrasion resistance index	106	105	101	102	103	102	100	95	91	90	100	93
	Wet-grip performance index	103	109	107	110	111	111	100	98	98	99	106	100
	Handling stability	6	6	6	6	6	6	6	5.75	6	6	5.5	6

TABLE 19
Examples in which an N,N-dialkyl-substituted carboxylic acid amide dialkyl acetal compound is used as a Terminal modifier
	Example	Comparative Example
	162	163	164	165	166	167	22	25	26	27	31	39
Formulation	Copolymer (8)	—	—	—	—	—	—	60	—	—	—	60	—
(parts by	Copolymer (12)	—	—	—	—	—	—	—	60	—	—	—	—
mass)	Copolymer (14)	—	—	—	—	—	—	—	—	60	—	—	—
	Copolymer (15)	—	—	—	—	—	—	—	—	—	60	—	—
	Copolymer (19)	—	—	—	—	—	—	—	—	—	—	20	—
	Copolymer (50)	60	—	—	—	—	—	—	—	—	—	—	—
	Copolymer (51)	—	60	—	—	—	—	—	—	—	—	—	—
	Copolymer (52)	—	—	60	—	—	—	—	—	—	—	—	—
	Copolymer (53)	—	—	—	60	—	—	—	—	—	—	—	—
	Copolymer (54)	—	—	—	—	60	—	—	—	—	—	—	—
	Copolymer (55)	—	—	—	—	—	60	—	—	—	—	—	—
	Copolymer (56)	—	—	—	—	—	—	—	—	—	—	—	60
	Natural rubber	20	20	20	20	20	20	20	20	20	20	20	20
	Polybutadiene rubber	20	20	20	20	20	20	20	20	20	20	—	20
	Carbon black	15	15	15	15	15	15	15	15	15	15	15	15
	Oil	25	25	25	25	25	25	25	25	25	25	25	25
	Silica 1 (N2SA: 80 m2/g)	—	—	—	—	—	—	—	—	—	—	—	—
	Silica 2 (N2SA: 110 m2/g)	60	60	60	60	60	60	60	60	60	60	60	60
	Silica 3 (N2SA: 160 m2/g)	15	15	15	15	15	15	15	15	15	15	15	15
	Silica 4 (N2SA: 200 m2/g)	—	—	—	—	—	—	—	—	—	—	—	—
	Silane coupling agent A	6	6	6	6	6	6	6	6	6	6	6	6
	Antioxidant	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5
	Stearic acid	2	2	2	2	2	2	2	2	2	2	2	2
	Zinc oxide	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5
	Wax	1	1	1	1	1	1	1	1	1	1	1	1
	Sulfur	2	2	2	2	2	2	2	2	2	2	2	2
	Vulcanization accelerator 1	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8
	Vulcanization accelerator 2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2
Evaluation	Mixing and kneading	112	114	113	113	109	115	100	97	96	94	98	98
	processability index
	Low-heat-build-property	121	114	112	118	117	109	100	93	100	99	107	94
	index
	tan δ peak temperature	−15	−15	−15	−15	−15	−15	−14	−16	−14	−14	−13	−15
	Rubber strength index	102	103	101	101	102	104	100	109	104	103	100	97
	Abrasion resistance index	107	106	102	101	102	101	100	95	91	90	100	92
	Wet-grip performance index	102	107	111	108	113	110	100	98	98	99	106	100
	Handling stability	6	6	6	6	6	6	6	5.75	6	6	5.5	6

TABLE 20
Examples in which a compound represented by the formula (IIId) is used as a Terminal modifier
			Comparative
		Example	Example
		168	169	170	171	172	173	174	175	176	177	40	41
Formulation	Copolymer (1)	60	—	—	—	—	—	—	—	—	—	—	—
(parts by	Copolymer (2)	—	60	—	—	—	—	—	—	—	—	—	—
mass)	Copolymer (3)	—	—	60	—	—	—	—	—	—	—	—	—
	Copolymer (4)	—	—	—	60	—	—	—	—	—	—	—	—
	Copolymer (5)	—	—	—	—	60	—	—	—	—	—	—	—
	Copolymer (6)	—	—	—	—	—	—	—	20	—	—	—	—
	Copolymer (7)	—	—	—	—	—	60	—	—	—	—	—	—
	Copolymer (8)	—	—	—	—	—	—	—	60	60	60	60	—
	Copolymer (9)	—	—	—	—	—	—	—	—	—	—	—	—
	Copolymer (10)	—	—	—	—	—	—	—	—	—	—	—	60
	Copolymer (11)	—	—	—	—	—	—	—	—	—	—	—	—
	Copolymer (12)	—	—	—	—	—	—	—	—	—	—	—	—
	Copolymer (13)	—	—	—	—	—	—	60	—	—	—	—	—
	Copolymer (14)	—	—	—	—	—	—	—	—	—	—	—	—
	Copolymer (15)	—	—	—	—	—	—	—	—	—	—	—	—
	Copolymer (16)	—	—	—	—	—	—	—	—	—	—	—	—
	Copolymer (17)	—	—	—	—	—	—	—	—	—	—	—	—
	Copolymer (18)	—	—	—	—	—	—	—	—	20	—	—	—
	Copolymer (19)	—	—	—	—	—	—	—	—	—	—	—	—
	Copolymer (20)	—	—	—	—	—	—	—	—	—	—	—	—
	Copolymer (21)	—	—	—	—	—	—	—	—	—	20	—	—
	Natural rubber	20	20	20	20	20	20	20	20	20	20	20	20
	Polybutadiene rubber	20	20	20	20	20	20	20	—	—	—	20	20
	Silica 2 (N2SA: 110 m2/g)	75	75	75	75	75	75	75	75	75	75	75	75
	Silane coupling agent A	6	6	6	6	6	6	6	6	6	6	6	6
	Carbon black	15	15	15	15	15	15	15	15	15	15	15	15
	Oil	25	25	25	25	25	25	25	25	25	25	25	25
	Coumarone indene resin 1	10	10	10	10	10	10	10	10	10	10	10	10
	(Tg: 90° C.)
	Coumarone indene resin 2	—	—	—	—	—	—	—	—	—	—	—	—
	(Tg: 10° C.)
	Coumarone indene resin 3	—	—	—	—	—	—	—	—	—	—	—	—
	(Tg: −30° C.)
	α-Methyl styrene resin	—	—	—	—	—	—	—	—	—	—	—	—
	(Tg: 95° C.)
	Antioxidant	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5
	Stearic acid	2	2	2	2	2	2	2	2	2	2	2	2
	Zinc oxide	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5
	Wax	1	1	1	1	1	1	1	1	1	1	1	1
	Sulfur	2	2	2	2	2	2	2	2	2	2	2	2
	Vulcanization accelerator 1	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8
	Vulcanization accelerator 2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2
Evaluation	Mixing and kneading process-	106	107	104	112	102	103	107	102	102	105	100	103
	ability index
	Low-heat-build-up property	127	129	128	140	137	139	110	127	132	113	100	98
	index
	tan δ peak temperature	−14	−14	−14	−14	−14	−14	−13	−14	−13	−13	−14	−14
	Rubber strength index	104	105	106	103	102	102	105	102	101	103	100	104
	Abrasion resistance index	102	103	102	100	101	103	102	101	103	99	100	100
	Wet-grip performance index	112	112	111	110	110	113	108	108	109	107	100	102
	Handling stability	6.25	6.25	6.25	6.25	6.25	6.25	6.25	6	6	6	6	6
	Comparative Example
			42	43	44	45	46	47	48	49	50	51
	Formulation	Copolymer (1)	—	—	—	—	—	—	—	—	—	—
	(parts by	Copolymer (2)	—	—	—	—	—	—	—	—	—	—
	mass)	Copolymer (3)	—	—	—	—	—	—	—	—	—	—
		Copolymer (4)	—	—	—	—	—	—	—	—	—	—
		Copolymer (5)	—	—	—	—	—	—	—	—	—	—
		Copolymer (6)	—	—	—	—	—	—	—	—	—	—
		Copolymer (7)	—	—	—	—	—	—	—	—	—	—
		Copolymer (8)	—	—	—	—	—	—	60	60	60	60
		Copolymer (9)	—	—	—	—	—	—	20	—	—	—
		Copolymer (10)	—	—	—	—	—	—	—	—	—	—
		Copolymer (11)	60	—	—	—	—	—	—	—	—	—
		Copolymer (12)	—	60	—	—	—	—	—	—	—	—
		Copolymer (13)	—	—	—	—	—	—	—	—	—	—
		Copolymer (14)	—	—	60	—	—	—	—	—	—	—
		Copolymer (15)	—	—	—	60	—	—	—	—	—	—
		Copolymer (16)	—	—	—	—	60	—	—	—	—	—
		Copolymer (17)	—	—	—	—	—	60	—	—	—	—
		Copolymer (18)	—	—	—	—	—	—	—	—	—	—
		Copolymer (19)	—	—	—	—	—	—	—	20	—	—
		Copolymer (20)	—	—	—	—	—	—	—	—	20	—
		Copolymer (21)	—	—	—	—	—	—	—	—	—	—
		Natural rubber	20	20	20	20	20	20	20	20	20	20
		Polybutadiene rubber	20	20	20	20	20	20	—	—	—	20
		Silica 2 (N2SA: 110 m2/g)	75	75	75	75	75	75	75	75	75	75
		Silane coupling agent A	6	6	6	6	6	6	6	6	6	6
		Carbon black	15	15	15	15	15	15	15	15	15	15
		Oil	25	25	25	25	25	25	25	25	25	25
		Coumarone indene resin 1	10	10	10	10	10	10	10	10	10	—
		(Tg: 90° C.)
		Coumarone indene resin 2	—	—	—	—	—	—	—	—	—	—
		(Tg: 10° C.)
		Coumarone indene resin 3	—	—	—	—	—	—	—	—	—	—
		(Tg: −30° C.)
		α-Methyl styrene resin	—	—	—	—	—	—	—	—	—	—
		(Tg: 95° C.)
		Antioxidant	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5
		Stearic acid	2	2	2	2	2	2	2	2	2	2
		Zinc oxide	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5
		Wax	1	1	1	1	1	1	1	1	1	1
		Sulfur	2	2	2	2	2	2	2	2	2	2
		Vulcanization accelerator 1	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8
		Vulcanization accelerator 2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2
	Evaluation	Mixing and kneading process-	99	98	97	95	94	94	98	99	103	97
		ability index
		Low-heat-build-up property	100	95	101	100	100	103	107	109	99	105
		index
		tan δ peak temperature	−14	−16	−14	−14	−14	−14	−14	−13	−13	−17
		Rubber strength index	102	107	102	101	103	101	98	98	100	94
		Abrasion resistance index	98	96	92	91	95	87	100	101	94	97
		Wet-grip performance index	102	97	98	99	98	101	107	106	104	98
		Handling stability	6	5.75	6	6	6	6	5.5	5.5	5.5	6.25

TABLE 21
Examples in which a compound represented by the formula (IV) is used as a Terminal modifier
			Comparative
		Example	Example
		178	179	180	181	182	183	184	40	43
Formulation	Copolymer (8)	—	—	—	—	—	—	—	60	—
(parts by	Copolymer (12)	—	—	—	—	—	—	—	—	60
mass)	Copolymer (14)	—	—	—	—	—	—	—	—	—
	Copolymer (15)	—	—	—	—	—	—	—	—	—
	Copolymer (19)	—	—	—	—	—	—	—	—	—
	Copolymer (22)	60	—	—	—	—	—	—	—	—
	Copolymer (23)	—	60	—	—	—	—	—	—	—
	Copolymer (24)	—	—	60	—	—	—	—	—	—
	Copolymer (25)	—	—	—	60	—	—	—	—	—
	Copolymer (26)	—	—	—	—	60	—	—	—	—
	Copolymer (27)	—	—	—	—	—	—	—	—	—
	Copolymer (28)	—	—	—	—	—	60	—	—	—
	Copolymer (29)	—	—	—	—	—	—	60	—	—
	Copolymer (30)	—	—	—	—	—	—	—	—	—
	Copolymer (31)	—	—	—	—	—	—	—	—	—
	Copolymer (32)	—	—	—	—	—	—	—	—	—
	Natural rubber	20	20	20	20	20	20	20	20	20
	Polybutadiene rubber	20	20	20	20	20	20	20	20	20
	Silica 2 (N2SA: 110 m2/g)	75	75	75	75	75	75	75	75	75
	Silane coupling agent A	6	6	6	6	6	6	6	6	6
	Carbon black	15	15	15	15	15	15	15	15	15
	Oil	25	25	25	25	25	25	25	25	25
	Coumarone indene resin 1 (Tg: 90° C.)	10	10	10	10	10	10	10	10	10
	Coumarone indene resin 2 (Tg: 10° C.)	—	—	—	—	—	—	—	—	—
	Coumarone indene resin 3 (Tg: −30° C.)	—	—	—	—	—	—	—	—	—
	α-Methyl styrene resin (Tg: 95° C.)	—	—	—	—	—	—	—	—	—
	Antioxidant	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5
	Stearic acid	2	2	2	2	2	2	2	2	2
	Zinc oxide	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5
	Wax	1	1	1	1	1	1	1	1	1
	Sulfur	2	2	2	2	2	2	2	2	2
	Vulcanization accelerator 1	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8
	Vulcanization accelerator 2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2
Evaluation	Mixing and kneading processability index	101	102	105	101	107	108	104	100	98
	Low-heat-build-property index	131	128	129	128	124	125	115	100	95
	tan δ peak temperature	−14	−14	−14	−14	−14	−14	−14	−14	−16
	Rubber strength index	108	107	106	108	109	106	110	100	107
	Abrasion resistance index	110	107	111	110	108	109	111	100	96
	Wet-grip performance index	108	108	107	109	110	108	108	100	97
	Handling stability	6	6	6	6	6	6	6	6	5.75
	Comparative Example	Example
			44	45	49	52	185	186	187
	Formulation	Copolymer (8)	—	—	60	—	60	60	60
	(parts by	Copolymer (12)	—	—	—	—	—	—	—
	mass)	Copolymer (14)	60	—	—	—	—	—	—
		Copolymer (15)	—	60	—	—	—	—	—
		Copolymer (19)	—	—	20	—	—	—	—
		Copolymer (22)	—	—	—	—	—	—	—
		Copolymer (23)	—	—	—	—	—	—	—
		Copolymer (24)	—	—	—	—	—	—	—
		Copolymer (25)	—	—	—	—	—	—	—
		Copolymer (26)	—	—	—	—	—	—	—
		Copolymer (27)	—	—	—	—	20	—	—
		Copolymer (28)	—	—	—	—	—	—	—
		Copolymer (29)	—	—	—	—	—	—	—
		Copolymer (30)	—	—	—	60	—	—	—
		Copolymer (31)	—	—	—	—	—	20	—
		Copolymer (32)	—	—	—	—	—	—	20
		Natural rubber	20	20	20	20	20	20	20
		Polybutadiene rubber	20	20	—	20	—	—	—
		Silica 2 (N2SA: 110 m2/g)	75	75	75	75	75	75	75
		Silane coupling agent A	6	6	6	6	6	6	6
		Carbon black	15	15	15	15	15	15	15
		Oil	25	25	25	25	25	25	25
		Coumarone indene resin 1 (Tg: 90° C.)	10	10	10	10	10	10	10
		Coumarone indene resin 2 (Tg: 10° C.)	—	—	—	—	—	—	—
		Coumarone indene resin 3 (Tg: −30° C.)	—	—	—	—	—	—	—
		α-Methyl styrene resin (Tg: 95° C.)	—	—	—	—	—	—	—
		Antioxidant	1.5	1.5	1.5	1.5	1.5	1.5	1.5
		Stearic acid	2	2	2	2	2	2	2
		Zinc oxide	2.5	2.5	2.5	2.5	2.5	2.5	2.5
		Wax	1	1	1	1	1	1	1
		Sulfur	2	2	2	2	2	2	2
		Vulcanization accelerator 1	1.8	1.8	1.8	1.8	1.8	1.8	1.8
		Vulcanization accelerator 2	1.2	1.2	1.2	1.2	1.2	1.2	1.2
	Evaluation	Mixing and kneading processability index	97	95	99	98	102	103	101
		Low-heat-build-property index	101	100	109	100	109	112	107
		tan δ peak temperature	−14	−14	−13	−14	−14	−14	−14
		Rubber strength index	102	101	98	103	105	106	105
		Abrasion resistance index	92	91	101	102	108	109	111
		Wet-grip performance index	98	99	106	105	111	109	107
		Handling stability	6	6	5.5	5.5	6	6	6

TABLE 22
Examples in which a compound represented by the formula (IIId) is used as a Terminal modifier
	Comparative
	Example	Example	Com. Ex.	Ex.	Com. Ex.
	40	43	173	188	189	190	191	53	192	54
Formulation	Copolymer (7)	—	—	60	60	60	60	60	30	70	100
(parts by	Copolymer (8)	60	—	—	—	—	—	—	—	—	—
mass)	Copolymer (12)	—	60	—	—	—	—	—	—	—	—
	Natural rubber	20	20	20	20	20	20	20	50	10	—
	Polybutadiene rubber	20	20	20	20	20	20	20	20	20	—
	Silica 2 (N2SA: 110 m2/g)	75	75	75	75	75	75	75	75	75	75
	Silane coupling agent A	6	6	6	6	6	6	6	6	6	6
	Carbon black	15	15	15	15	15	15	15	15	15	15
	Oil	25	25	25	25	25	25	25	25	25	25
	Coumarone indene resin 1 (Tg: 90° C.)	10	10	10	—	20	10	10	10	10	10
	Coumarone indene resin 2 (Tg: 10° C.)	—	—	—	—	—	5	—	—	—	—
	Coumarone indene resin 3 (Tg: −30° C.)	—	—	—	—	—	—	5	—	—	—
	α-Methyl styrene resin (Tg: 95° C.)	—	—	—	10	—	—	—	—	—	—
	Antioxidant	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5
	Stearic acid	2	2	2	2	2	2	2	2	2	2
	Zinc oxide	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5
	Wax	1	1	1	1	1	1	1	1	1	1
	Sulfur	2	2	2	2	2	2	2	2	2	2
	Vulcanization accelerator 1	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8
	Vulcanization accelerator 2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2
Evaluation	Mixing and kneading processability index	100	98	103	103	115	109	111	124	107	80
	Low-heat-build-property index	100	95	139	138	134	136	139	130	140	128
	tan δ peak temperature	−14	−16	−14	−14	−14	−15	−16	−20	−13	−11
	Rubber strength index	100	107	102	102	108	106	107	132	101	85
	Abrasion resistance index	100	96	103	99	101	101	104	114	107	92
	Wet-grip performance index	100	97	113	116	123	114	116	92	114	127
	Handling stability	6	5.75	6.25	6.25	6	6	6	5.5	6.5	5.5

TABLE 23
Examples in which a compound represented by the formula (IIIb) is used as a Terminal modifier
	Example
		193	194	195	196	197	198	199	200	201
Formulation	Copolymer (8)	—	—	—	—	—	—	—	—	—
(parts by	Copolymer (12)	—	—	—	—	—	—	—	—	—
mass)	Copolymer (14)	—	—	—	—	—	—	—	—	—
	Copolymer (15)	—	—	—	—	—	—	—	—	—
	Copolymer (19)	—	—	—	—	—	—	—	—	—
	Copolymer (33)	60	—	—	—	—	—	—	—	—
	Copolymer (34)	—	60	—	—	—	—	—	—	—
	Copolymer (35)	—	—	60	—	—	—	—	—	—
	Copolymer (36)	—	—	—	60	—	—	—	—	—
	Copolymer (37)	—	—	—	—	60	—	—	—	—
	Copolymer (38)	—	—	—	—	—	60	—	—	—
	Copolymer (39)	—	—	—	—	—	—	60	—	—
	Copolymer (40)	—	—	—	—	—	—	—	60	—
	Copolymer (41)	—	—	—	—	—	—	—	—	60
	Copolymer (42)	—	—	—	—	—	—	—	—	—
	Natural rubber	20	20	20	20	20	20	20	20	20
	Polybutadiene rubber	20	20	20	20	20	20	20	20	20
	Silica 2 (N2SA: 110 m2/g)	75	75	75	75	75	75	75	75	75
	Silane coupling agent A	6	6	6	6	6	6	6	6	6
	Carbon black	15	15	15	15	15	15	15	15	15
	Oil	25	25	25	25	25	25	25	25	25
	Coumarone indene resin 1 (Tg: 90° C.)	10	10	10	10	10	10	10	10	10
	Coumarone indene resin 2 (Tg: 10° C.)	—	—	—	—	—	—	—	—	—
	Coumarone indene resin 3 (Tg: −30° C.)	—	—	—	—	—	—	—	—	—
	α-Methyl styrene resin (Tg: 95° C.)	—	—	—	—	—	—	—	—	—
	Antioxidant	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5
	Stearic acid	2	2	2	2	2	2	2	2	2
	Zinc oxide	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5
	Wax	1	1	1	1	1	1	1	1	1
	Sulfur	2	2	2	2	2	2	2	2	2
	Vulcanization accelerator 1	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8
	Vulcanization accelerator 2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2
Evaluation	Mixing and kneading processability index	104	109	105	104	105	109	104	105	103
	Low-heat-build-property index	121	117	118	111	121	108	118	105	103
	tan δ peak temperature	−15	−15	−15	−15	−15	−15	−15	−15	−15
	Rubber strength index	109	110	109	111	108	111	109	113	111
	Abrasion resistance index	102	102	101	104	102	103	101	104	103
	Wet-grip performance index	103	103	102	112	102	111	105	108	107
	Handling stability	6.25	6	6	6	6.25	6.25	6	6	6
	Comparative Example
			40	43	44	45	49	55
	Formulation	Copolymer (8)	60	—	—	—	60	—
	(parts by	Copolymer (12)	—	60	—	—	—	—
	mass)	Copolymer (14)	—	—	60	—	—	—
		Copolymer (15)	—	—	—	60	—	—
		Copolymer (19)	—	—	—	—	20	—
		Copolymer (33)	—	—	—	—	—	—
		Copolymer (34)	—	—	—	—	—	—
		Copolymer (35)	—	—	—	—	—	—
		Copolymer (36)	—	—	—	—	—	—
		Copolymer (37)	—	—	—	—	—	—
		Copolymer (38)	—	—	—	—	—	—
		Copolymer (39)	—	—	—	—	—	—
		Copolymer (40)	—	—	—	—	—	—
		Copolymer (41)	—	—	—	—	—	—
		Copolymer (42)	—	—	—	—	—	60
		Natural rubber	20	20	20	20	20	20
		Polybutadiene rubber	20	20	20	20	—	20
		Silica 2 (N2SA: 110 m2/g)	75	75	75	75	75	75
		Silane coupling agent A	6	6	6	6	6	6
		Carbon black	15	15	15	15	15	15
		Oil	25	25	25	25	25	25
		Coumarone indene resin 1 (Tg: 90° C.)	10	10	10	10	10	10
		Coumarone indene resin 2 (Tg: 10° C.)	—	—	—	—	—	—
		Coumarone indene resin 3 (Tg: −30° C.)	—	—	—	—	—	—
		α-Methyl styrene resin (Tg: 95° C.)	—	—	—	—	—	—
		Antioxidant	1.5	1.5	1.5	1.5	1.5	1.5
		Stearic acid	2	2	2	2	2	2
		Zinc oxide	2.5	2.5	2.5	2.5	2.5	2.5
		Wax	1	1	1	1	1	1
		Sulfur	2	2	2	2	2	2
		Vulcanization accelerator 1	1.8	1.8	1.8	1.8	1.8	1.8
		Vulcanization accelerator 2	1.2	1.2	1.2	1.2	1.2	1.2
	Evaluation	Mixing and kneading processability index	100	98	97	95	99	96
		Low-heat-build-property index	100	95	101	100	109	97
		tan δ peak temperature	−14	−16	−14	−14	−13	−15
		Rubber strength index	100	107	102	101	98	108
		Abrasion resistance index	100	96	92	91	101	93
		Wet-grip performance index	100	97	98	99	106	102
		Handling stability	6	5.75	6	6	5.5	6

TABLE 24
Examples in which a compound containing an alkoxysilyl group, a
nitrogen atom and a carbonyl group is used as a Terminal modifier
	Example	Comparative Example
	202	203	204	205	206	207	40	43	44	45	49	56
Formulation	Copolymer (8)	—	—	—	—	—	—	60	—	—	—	60	—
(parts by	Copolymer (12)	—	—	—	—	—	—	—	60	—	—	—	—
mass)	Copolymer (14)	—	—	—	—	—	—	—	—	60	—	—	—
	Copolymer (15)	—	—	—	—	—	—	—	—	—	60	—	—
	Copolymer (19)	—	—	—	—	—	—	—	—	—	—	20	—
	Copolymer (43)	60	—	—	—	—	—	—	—	—	—	—	—
	Copolymer (44)	—	60	—	—	—	—	—	—	—	—	—	—
	Copolymer (45)	—	—	60	—	—	—	—	—	—	—	—	—
	Copolymer (46)	—	—	—	60	—	—	—	—	—	—	—	—
	Copolymer (47)	—	—	—	—	60	—	—	—	—	—	—	—
	Copolymer (48)	—	—	—	—	—	60	—	—	—	—	—	—
	Copolymer (49)	—	—	—	—	—	—	—	—	—	—	—	60
	Natural rubber	20	20	20	20	20	20	20	20	20	20	20	20
	Polybutadiene rubber	20	20	20	20	20	20	20	20	20	20	—	20
	Silica 2 (N2SA: 110 m2/g)	75	75	75	75	75	75	75	75	75	75	75	75
	Silane coupling agent A	6	6	6	6	6	6	6	6	6	6	6	6
	Carbon black	15	15	15	15	15	15	15	15	15	15	15	15
	Oil	25	25	25	25	25	25	25	25	25	25	25	25
	Coumarone indene resin 1	10	10	10	10	10	10	10	10	10	10	10	10
	(Tg: 90° C.)
	Coumarone indene resin 2	—	—	—	—	—	—	—	—	—	—	—	—
	(Tg: 10° C.)
	Coumarone indene resin 3	—	—	—	—	—	—	—	—	—	—	—	—
	(Tg: −30° C.)
	α-Methyl styrene resin	—	—	—	—	—	—	—	—	—	—	—	—
	(Tg: 95° C.)
	Antioxidant	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5
	Stearic acid	2	2	2	2	2	2	2	2	2	2	2	2
	Zinc oxide	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5
	Wax	1	1	1	1	1	1	1	1	1	1	1	1
	Sulfur	2	2	2	2	2	2	2	2	2	2	2	2
	Vulcanization accelerator 1	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8
	Vulcanization accelerator 2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2
Evaluation	Mixing and kneading	108	107	105	104	102	107	100	98	97	95	99	98
	processability index
	Low-heat-build-property	116	108	115	112	116	107	100	95	101	100	109	94
	index
	tan δ peak temperature	−15	−15	−15	−15	−15	−15	−14	−16	−14	−14	−13	−15
	Rubber strength index	106	108	106	107	106	109	100	107	102	101	98	107
	Abrasion resistance index	107	106	102	103	104	103	100	96	92	91	101	92
	Wet-grip performance index	102	108	106	109	110	110	100	97	98	99	106	100
	Handling stability	6	6	6	6	6	6	6	5.75	6	6	5.5	6

TABLE 25
Examples in which an N,N-dialkyl-substituted carboxylic acid amide dialkyl acetal compound is used as a Terminal modifier
	Example	Comparative Example
	208	209	210	211	212	213	40	43	44	45	49	57
Formulation	Copolymer (8)	—	—	—	—	—	—	60	—	—	—	60	—
(parts by	Copolymer (12)	—	—	—	—	—	—	—	60	—	—	—	—
mass)	Copolymer (14)	—	—	—	—	—	—	—	—	60	—	—	—
	Copolymer (15)	—	—	—	—	—	—	—	—	—	60	—	—
	Copolymer (19)	—	—	—	—	—	—	—	—	—	—	20	—
	Copolymer (50)	60	—	—	—	—	—	—	—	—	—	—	—
	Copolymer (51)	—	60	—	—	—	—	—	—	—	—	—	—
	Copolymer (52)	—	—	60	—	—	—	—	—	—	—	—	—
	Copolymer (53)	—	—	—	60	—	—	—	—	—	—	—	—
	Copolymer (54)	—	—	—	—	60	—	—	—	—	—	—	—
	Copolymer (55)	—	—	—	—	—	60	—	—	—	—	—	—
	Copolymer (56)	—	—	—	—	—	—	—	—	—	—	—	60
	Natural rubber	20	20	20	20	20	20	20	20	20	20	20	20
	Polybutadiene rubber	20	20	20	20	20	20	20	20	20	20	—	20
	Silica 2 (N2SA: 110 m2/g)	75	75	75	75	75	75	75	75	75	75	75	75
	Silane coupling agent A	6	6	6	6	6	6	6	6	6	6	6	6
	Carbon black	15	15	15	15	15	15	15	15	15	15	15	15
	Oil	25	25	25	25	25	25	25	25	25	25	25	25
	Coumarone indene resin 1	10	10	10	10	10	10	10	10	10	10	10	10
	(Tg: 90° C.)
	Coumarone indene resin 2	—	—	—	—	—	—	—	—	—	—	—	—
	(Tg: 10° C.)
	Coumarone indene resin 3	—	—	—	—	—	—	—	—	—	—	—	—
	(Tg: −30° C.)
	α-Methyl styrene resin	—	—	—	—	—	—	—	—	—	—	—	—
	(Tg: 95° C.)
	Antioxidant	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5	1.5
	Stearic acid	2	2	2	2	2	2	2	2	2	2	2	2
	Zinc oxide	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5	2.5
	Wax	1	1	1	1	1	1	1	1	1	1	1	1
	Sulfur	2	2	2	2	2	2	2	2	2	2	2	2
	Vulcanization accelerator 1	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8	1.8
	Vulcanization accelerator 2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2	1.2
Evaluation	Mixing and kneading	105	107	106	106	102	108	100	98	97	95	99	96
	processability index
	Low-heat-build-property	117	110	108	114	113	106	100	95	101	100	109	94
	index
	tan δ peak temperature	−15	−15	−15	−15	−15	−15	−14	−16	−14	−14	−13	−15
	Rubber strength index	107	108	106	106	107	109	100	107	102	101	98	107
	Abrasion resistance index	108	107	103	102	103	102	100	96	92	91	101	91
	Wet-grip performance index	101	106	110	107	112	109	100	97	98	99	106	100
	Handling stability	6	6	6	6	6	6	6	5.75	6	6	5.5	6

As shown in Tables 6 to 25, since each of the rubber compositions of the examples contains a specific amount or more of SBR as well as a specific amount of a silica and a specific amount of a conjugated diene copolymer having a specific amine structure at an initiation terminal, a structural unit derived from a silicon-containing compound at a main chain, and a structural unit derived from a compound containing a nitrogen atom and/or a silicon atom at a termination terminal, these rubber compositions exhibited a balanced improvement in processability, fuel economy, rubber strength, abrasion resistance, wet-grip performance, and handling stability as compared to the rubber compositions of the comparative examples. Moreover, comparison between the conjugated diene polymer in which the three sites (the initiation terminal, main chain, and termination terminal) are modified by specific compounds, and a copolymer in which only one of the initiation terminal, main chain, and termination terminal is modified shows that modification of the three sites (the initiation terminal, main chain, and termination terminal) synergistically increases the effects of improving those properties.

The rubber compositions of Examples 21 to 35 and 37 to 213, each containing the conjugated diene polymer together with at least one of a mercapto group-containing silane coupling agent, a combination of two kinds of silica having specific nitrogen adsorption specific surface areas, and a solid resin having a specific glass transition temperature, exhibited greatly improved properties.

Each of the rubber compositions of Comparative Example 8, 29, and 47 contains, instead of the conjugated diene polymer, the copolymer (17) which has a structural unit derived from a silicon-containing compound at a main chain and a structural unit derived from a compound containing a nitrogen atom and/or a silicon atom at a termination terminal but does not have a specific amine structure at an initiation terminal. The rubber compositions of Comparative Examples 8, 29, and 47 have inferior properties to those in the examples, and furthermore, have poor abrasion resistance and processability as compared to those of the standard comparative examples.

The rubber composition of Comparative Example 53 containing the conjugated rubber composition and a small amount of SBR was inferior in wet-grip performance and handling stability to the rubber composition of Comparative Example 1.

Each of the rubber compositions of Comparative Examples 15, 36, and 54 contains too large an amount of the conjugated diene polymer. Thus, the abrasion resistance and other properties were very poor.

Claims

1. A rubber composition, comprising, based on 100% by mass of a rubber component, not less than 35% by mass of styrene-butadiene rubber, the rubber composition comprising

a conjugated diene polymer, and

a silica having a nitrogen adsorption specific surface area of 40 to 400 m²/g,

the conjugated diene polymer being obtained by polymerizing a monomer component including a conjugated diene compound and a silicon-containing vinyl compound in the presence of a polymerization initiator represented by the following formula (I):

2. The rubber composition according to claim 1,

wherein R¹¹ in the formula (I) is a group represented by the following formula (Ia):

3. The rubber composition according to claim 2,

wherein R¹⁴ in the formula (Ia) is a hydrocarbylene group comprising from one to ten isoprene-derived structural unit(s).

4. The rubber composition according to claim 1,

wherein the conjugated diene polymer contains a structural unit derived from an aromatic vinyl compound.

5. The rubber composition according to claim 1,

wherein the silica includes silica (1) having a nitrogen adsorption specific surface area of at least 50 m²/g but less than 120 m²/g, and silica (2) having a nitrogen adsorption specific surface area of not less than 120 m²/g.

6. The rubber composition according to claim 1, comprising

a solid resin having a glass transition temperature of 60 to 120° C. in an amount of 1 to 30 parts by mass for each 100 parts by mass of the rubber component.

7. The rubber composition according to claim 1,

wherein the silica includes silica (1) having a nitrogen adsorption specific surface area of at least 50 m²/g but less than 120 m²/g, and silica (2) having a nitrogen adsorption specific surface area of not less than 120 m²/g, and

the rubber composition comprises a solid resin having a glass transition temperature of 60 to 120° C. in an amount of 1 to 30 parts by mass for each 100 parts by mass of the rubber component.

8. The rubber composition according to claim 1, comprising

a mercapto group-containing silane coupling agent in an amount of 0.5 to 20 parts by mass for each 100 parts by mass of the silica.

9. The rubber composition according to claim 1,

wherein the rubber composition comprises a mercapto group-containing silane coupling agent in an amount of 0.5 to 20 parts by mass for each 100 parts by mass of the silica, and

the silica includes silica (1) having a nitrogen adsorption specific surface area of at least 50 m²/g but less than 120 m²/g, and silica (2) having a nitrogen adsorption specific surface area of not less than 120 m²/g.

10. The rubber composition according to claim 1, comprising

a mercapto group-containing silane coupling agent in an amount of 0.5 to 20 parts by mass for each 100 parts by mass of the silica, and

a solid resin having a glass transition temperature of 60 to 120° C. in an amount of 1 to 30 parts by mass for each 100 parts by mass of the rubber component.

11. The rubber composition according to claim 1,

wherein the rubber composition comprises a mercapto group-containing silane coupling agent in an amount of 0.5 to 20 parts by mass for each 100 parts by mass of the silica,

the silica includes silica (1) having a nitrogen adsorption specific surface area of at least 50 m²/g but less than 120 m²/g, and silica (2) having a nitrogen adsorption specific surface area of not less than 120 m²/g, and

the rubber composition comprises a solid resin having a glass transition temperature of 60 to 120° C. in an amount of 1 to 30 parts by mass for each 100 parts by mass of the rubber component.

12. The rubber composition according to claim 1,

wherein the rubber composition comprises a mercapto group-containing silane coupling agent in an amount of 0.5 to 20 parts by mass for each 100 parts by mass of the silica, and

the silane coupling agent is at least one of a compound represented by the formula (1) below, and a compound containing a linking unit A represented by the formula (2) below and a linking unit B represented by the formula (3) below,

13. The rubber composition according to claim 1,

wherein the silica includes silica (1) having a nitrogen adsorption specific surface area of at least 50 m²/g but less than 120 m²/g, and silica (2) having a nitrogen adsorption specific surface area of not less than 120 m²/g, and

the nitrogen adsorption specific surface areas and amounts of the silica (1) and the silica (2) satisfy the following inequalities:

(nitrogen adsorption specific surface area of silica (2))/(nitrogen adsorption specific surface area of silica (1))≧1.4, and

(amount of silica (1))×0.06≦(amount of silica (2))≦(amount of silica (1))×15.

14. The rubber composition according to claim 1, comprising at least one of

at least one liquid resin having a glass transition temperature of −40 to 20° C. selected from the group consisting of aromatic petroleum resins, terpene resins, and rosin resins, and

a plasticizer having a glass transition temperature of −40 to 20° C.,

wherein a combined amount of the liquid resin and the plasticizer is 1 to 30 parts by mass for each 100 parts by mass of the rubber component.

15. The rubber composition according to claim 1,

wherein the rubber composition has a tan δ peak temperature of not lower than −16° C.

16. A tread, formed from the rubber composition according to claim 1.

17. A pneumatic tire, formed from the rubber composition according to claim 1.

18. The pneumatic tire according to claim 17, wherein the wet grip performance index is equal to or between 106 and 125 and the handling stability is equal to or between 6 and 6.5.